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7-Bromothieno[3,2-d]pyrimidin-2-amine synthesis

6synthesis methods
-

Yield:1293987-58-2 60%

Reaction Conditions:

with ammonia in isopropyl alcohol at 100; for 48 h;Sealed reactor;

Steps:

19.1

7-Bromo-2-chlorothieno[3,2-d]pyrimidine (1.0 g, 4.03 mmol) was dissolved in 2.0 M ammonia isopropanol (10 mL) and stirred at 100 °C for 48 hours in a sealed reactor. The reaction mixture was cooled to room temperature and then concentrated. Purification by chromatography (50% ethyl acetate/hexane) yielded a brown solid compound (560 mg, 60% yield). [0253] 1H NMR (400 MHz, DMSO-d 6) δ 8.95 (s, 1H), 8.36 (s, 1H), 6.89 (s, 2H), MS m/z: 230.26, 232.26 [M+1].

References:

WO2011/49332,2011,A2 Location in patent:Page/Page column 29

41102-02-7 Synthesis
7-bromothieno[3,2-d]pyrimidine-2,4(1H,3H)-dione

41102-02-7
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7-Bromothieno[3,2-d]pyrimidin-2-amine

1293987-58-2
7 suppliers
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