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16234-14-3

Thieno[3,2-d]pyrimidine, 2,4-dichloro-

Thieno[3,2-d]pyrimidine, 2,4-dichloro-

Another Name:
CasNo.: 16234-14-3
MF: C6H2Cl2N2S
MW: 205.067
Storage:
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ch_Name: Thieno[3,2-d]pyrimidine, 2,4-dichloro-
English name: Thieno[3,2-d]pyrimidine, 2,4-dichloro-
CasNo.: 16234-14-3
MF: C6H2Cl2N2S
MW: 205.067

Reliable factory customized supply Thieno[3,2-d]pyrimidine, 2,4-dichloro- 16234-14-3

  • Molecular Formula:C6H2Cl2N2S
  • Molecular Weight:205.067
  • Melting Point:136.0 to 140.0 °C 
  • Boiling Point:274.804 °C at 760 mmHg 
  • PKA:-0.72±0.40(Predicted) 
  • Flash Point:119.997 °C 
  • PSA:54.02000 
  • Density:1.662 g/cm3 
  • LogP:2.99810 

16234-14-3 Relevant articles

Discovery of novel and potent PARP/PI3K dual inhibitors for the treatment of cancer

Wu, Zhengyang,Bai, Ying,Jin, Jiaming,Jiang, Teng,Shen, Hui,Ju, Qiurong,Zhu, Qihua,Xu, Yungen

, (2021/03/19)

PARP inhibitors have achieved great succ...

PARP-1/PI3K double-target inhibitor or pharmaceutically acceptable salt thereof, preparation method and application thereof

-

Paragraph 0157; 0162-0164; 0191; 0195-0197, (2021/07/01)

The invention discloses a PARP-1/PI3K do...

Design, synthesis and biological evaluation of novel 2,4-bismorpholinothieno[3,2-d]pyrimidine and 2-morpholinothieno[3,2-d]pyrimidinone derivatives as potent antitumor agents

Ye, Tianyu,Han, Yufei,Wang, Ruxin,Yan, Pingzhen,Chen, Shaowei,Hou, Yunlei,Zhao, Yanfang

, (2020/04/15)

To develop novel therapeutic agents with...

COMBINATION THERAPY WITH A PHOSPHOINOSITIDE 3-KINASE INHIBITOR WITH A ZINC BINDING MOIETY

-

Paragraph 0087; 0103, (2020/04/09)

The invention provides a method of treat...

16234-14-3 Process route

1H-thieno[3,2-d]pyrimidine-2,4-dione
16233-51-5

1H-thieno[3,2-d]pyrimidine-2,4-dione

2,4-dichlorothieno[3,2-d]pyrimidine
16234-14-3

2,4-dichlorothieno[3,2-d]pyrimidine

Conditions
Conditions Yield
With N-ethyl-N,N-diisopropylamine; trichlorophosphate; for 2h; Heating / reflux;
100%
With N,N-dimethyl-formamide; trichlorophosphate; at 110 ℃; for 2h;
95.4%
With N,N-diethylaniline; trichlorophosphate; at 105 ℃; for 16h;
92%
With N,N-dimethyl-aniline; trichlorophosphate; In acetonitrile; at 20 - 85 ℃; for 26h; Inert atmosphere; Large scale;
89%
With N-ethyl-N,N-diisopropylamine; trichlorophosphate; for 2h; Reflux;
87.3%
With N,N-dimethyl-aniline; trichlorophosphate; In acetonitrile; at 0 - 85 ℃; for 48h;
84%
With trichlorophosphate; at 80 ℃; for 8h;
84.7%
With N,N-dimethyl-aniline; trichlorophosphate; In acetonitrile; at 20 - 85 ℃; for 24h; Cooling;
83%
With trichlorophosphate; In N,N-dimethyl-aniline; acetonitrile; at 15 - 85 ℃; for 24h;
83%
With N,N-dimethyl-aniline; trichlorophosphate; In acetonitrile; at 85 ℃; for 24h;
83%
With trichlorophosphate; at 105 - 110 ℃; for 16h; Inert atmosphere;
82%
With trichlorophosphate; for 16h; Inert atmosphere; Reflux;
82%
With triethylamine; trichlorophosphate; at 0 ℃; for 8h; Reflux;
81.7%
With trichlorophosphate; for 8h; Reflux;
81.4%
With N,N-dimethyl-aniline; trichlorophosphate; In acetonitrile; at 50 - 85 ℃; Large scale;
79.6%
With trichlorophosphate; for 6h; Heating / reflux;
75%
With trichlorophosphate; for 6h; Heating / reflux;
75%
With trichlorophosphate; for 6h; Heating / reflux;
75%
With trichlorophosphate; for 6h; Heating / reflux;
75%
1H-thieno[3,2-d]pyrimidine-2,4-dione; With trichlorophosphate; for 6h; Heating / reflux;
With water;
75%
With trichlorophosphate; In acetonitrile; for 24h; Heating / reflux;
75%
With trichlorophosphate;
75%
With trichlorophosphate; for 6h; Reflux;
75%
With trichlorophosphate; for 6h; Reflux;
75%
With trichlorophosphate; In acetonitrile; for 24h; Heating / reflux;
75%
With trichlorophosphate; for 6h; Heating / reflux;
75%
With trichlorophosphate; for 6h; Heating / reflux;
75%
With trichlorophosphate; for 10h; Reflux;
74%
With trichlorophosphate; for 5h; Reflux;
74%
With trichlorophosphate; for 10h; Reflux;
74%
With trichlorophosphate; at 110 ℃; for 5h;
74%
With trichlorophosphate; for 10h; Reflux;
74%
With trichlorophosphate; at 200 ℃; for 3h;
73.3%
With trichlorophosphate; for 8h; Inert atmosphere; Heating;
73%
With N,N-dimethyl-formamide; trichlorophosphate; for 8h; Reflux;
72%
With N,N-dimethyl-formamide; trichlorophosphate; for 8h; Reflux;
72%
With trichlorophosphate; In N,N-dimethyl-formamide; for 8h; Reflux;
72%
With trichlorophosphate; for 10h; Reflux;
70%
With N,N-dimethyl-aniline; trichlorophosphate; for 16h; Reflux;
67%
With trichlorophosphate; for 8h; Reflux;
67%
With trichlorophosphate; at 106 ℃; for 3h; Inert atmosphere;
41%
With phosphorus pentachloride; trichlorophosphate; at 135 ℃; for 5h;
36%
With trichlorophosphate; at 116 ℃; for 5h;
28%
With 2,3-Dimethylaniline; trichlorophosphate; In diethyl ether; water;
With N,N-diethylaniline; trichlorophosphate; at 100 ℃; for 12h;
With N,N-dimethyl-formamide; trichlorophosphate; for 8h; Reflux;
With trichlorophosphate; for 6h; Reflux;
16.9 g
With N,N-dimethyl-formamide; trichlorophosphate; Reflux;
With trichlorophosphate; at 100 ℃; for 10h;
With phosphorus pentachloride; trichlorophosphate; at 120 ℃; for 6h; Inert atmosphere;
With trichlorophosphate; at 100 ℃; for 10h;
With N,N-dimethyl-formamide; trichlorophosphate; for 8h; Reflux;
With trichlorophosphate; for 8h; Reflux;
2,4-dihydroxythieno[3,2-d]pyrimidine
16233-51-5

2,4-dihydroxythieno[3,2-d]pyrimidine

2,4-dichlorothieno[3,2-d]pyrimidine
16234-14-3

2,4-dichlorothieno[3,2-d]pyrimidine

Conditions
Conditions Yield
With trichlorophosphate; at 100 ℃; Product distribution / selectivity;
100%
With trichlorophosphate; at 120 ℃;
100%
With trichlorophosphate; In acetonitrile; for 4h; Reflux;
95%
With trichlorophosphate; for 14h; Heating / reflux;
93%
With trichlorophosphate; for 14h; Heating / reflux;
93%
With trichlorophosphate; In acetonitrile; at 90 ℃; for 8h;
81.4%
With 1-methyl-pyrrolidin-2-one; trichlorophosphate; In toluene; Reflux; Inert atmosphere;
80%
With 1-methyl-pyrrolidin-2-one; trichlorophosphate; In toluene; for 16h; Reflux;
80%
With trichlorophosphate; In acetonitrile; for 48h; Reflux;
79%
With N,N-dimethyl-aniline; trichlorophosphate; In acetonitrile; at 80 - 85 ℃; for 72h;
79%
With trichlorophosphate; In N,N-dimethyl-formamide; at 120 ℃; for 3h;
79.6%
With N,N-dimethyl-aniline; trichlorophosphate; for 14h; Heating / reflux;
74.4%
With trichlorophosphate; for 10h; Reflux;
70.5%
With trichlorophosphate; for 10h; Reflux;
70.5%
With trichlorophosphate; for 12h; Reflux;
69%
With N,N-dimethyl-formamide; trichlorophosphate; for 12h; Reflux;
69.8%
With P,P-dichlorophenylphosphine oxide; at 170 ℃; for 2h;
66%
With P,P-dichlorophenylphosphine oxide; at 170 ℃; for 2h;
66%
With P,P-dichlorophenylphosphine oxide; at 180 ℃; for 4h;
60%
With trichlorophosphate; In N,N-dimethyl-aniline; for 3h;
51.2%
With trichlorophosphate;

16234-14-3 Upstream products

  • 16233-51-5
    16233-51-5

    1H-thieno[3,2-d]pyrimidine-2,4-dione

  • 16233-51-5
    16233-51-5

    thienoyleneurea

  • 16233-51-5
    16233-51-5

    2,4-dihydroxythieno[3,2-d]pyrimidine

  • 22288-78-4
    22288-78-4

    Methyl 3-aminothiophene-2-carboxylate

16234-14-3 Downstream products

  • 147972-18-7
    147972-18-7

    4'-[[[2-chlorothieno-[3,2-d]pyrimidin-4-yL]amino]methyl][1,1'-biphenyl]-2-carboxylic acid methyl ester

  • 152943-20-9
    152943-20-9

    2-(3,4-Dimethoxyphenethylamino)-4-(1,2,3,4-tetrahydro-6,7-dimethoxyisoquinol-2-yl)thieno[3,2-d]pyrimidine hydrochloride

  • 1024603-85-7
    1024603-85-7

    4-((2-chlorothiophene[3,2-d]pyrimidin-4-yl)oxy)-3,5-dimethylbenzonitrile

  • 1024603-87-9
    1024603-87-9

    2-chloro-N-mesitylthieno[3,2-d]pyrimidin-4-amine

No data available
No data available
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