| Identification | Back Directory | [Name]
4-CHLORO-5-METHYLTHIENO[2,3-D]PYRIMIDINE | [CAS]
43088-67-1 | [Synonyms]
BUTTPARK 46\18-75
4-Chloro-5-Methylthieno[2...
4-CHLORO-5-METHYLTHIENO[2,3-D]PYRIMIDINE
Thieno[2,3-d]pyrimidine, 4-chloro-5-methyl-
4-Chloro-5-methylthieno[2,3-d]pyrimidine ,97%
4-CHLORO-5-METHYLTHIENO[2,3-D]PYRIMIDINE ISO 9001：2015 REACH | [Molecular Formula]
C7H5ClN2S | [MDL Number]
MFCD00205201 | [MOL File]
43088-67-1.mol | [Molecular Weight]
184.65 |
| Chemical Properties | Back Directory | [Melting point ]
137 °C | [Boiling point ]
301.3±37.0 °C(Predicted) | [density ]
1.445±0.06 g/cm3(Predicted) | [storage temp. ]
under inert gas (nitrogen or Argon) at 2-8°C | [pka]
0.71±0.40(Predicted) |
| Hazard Information | Back Directory | [Synthesis]
Step 2. Preparation of 4-chloro-5-methylthieno[2,3-d]pyrimidine: 5-methylthieno[2,3-d]pyrimidin-4(3H)-one (1.4 g, 8.42 mmol) prepared in Step 1 was dissolved in phosphorochloridic acid (5 mL). Subsequently, the reaction mixture was stirred at 110°C for 1 hour. Upon completion of the reaction, the reaction mixture was slowly poured into a mixture of ice water and chloroform and washed sequentially with water and saturated aqueous sodium bicarbonate. The organic layers were combined and concentrated under reduced pressure. The residue was purified by recrystallization (hexane/ethyl acetate mixed solvent) to give 590 mg (yield: 39%) of the target product 4-chloro-5-methylthieno[2,3-d]pyrimidine as a yellow solid.1H NMR (400 MHz, CDCl3): δ 8.81 (s, 1H), 7.24 (s, 1H), 2.70 (s, 3H). | [References]
[1] Patent: WO2007/102679, 2007, A1. Location in patent: Page/Page column 49
[2] Bioorganic and Medicinal Chemistry Letters, 2016, vol. 26, # 6, p. 1525 - 1528 |
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