4-Chloro-5-methylthieno[2,3-d]pyrimidine → 1-(3-Fluoro-4-(5-methyl-4a,7a-dihydrothieno[2,3-d]pyrimidin-4-yloxy)phenyl)-3-(2-(4-fluorophenyl)acetyl)thiourea

HRID 347466

반응식

HRID 347466 반응식
Cl[C:2]1[C:3]2[C:10]([CH3:11])=[CH:9][S:8][C:4]=2[N:5]=[CH:6][N:7]=1.[F:12][C:13]1[CH:14]=[C:15]([NH:20][C:21]([NH:23][C:24](=[O:33])[CH2:25][C:26]2[CH:31]=[CH:30][C:29]([F:32])=[CH:28][CH:27]=2)=[S:22])[CH:16]=[CH:17][C:18]=1[OH:19]>>[F:12][C:13]1[CH:14]=[C:15]([NH:20][C:21]([NH:23][C:24](=[O:33])[CH2:25][C:26]2[CH:27]=[CH:28][C:29]([F:32])=[CH:30][CH:31]=2)=[S:22])[CH:16]=[CH:17][C:18]=1[O:19][C:2]1[CH:3]2[C:10]([CH3:11])=[CH:9][S:8][CH:4]2[N:5]=[CH:6][N:7]=1

참가 물질

3

실험 절차

In a similar manner as described for the preparation of Example 10, the title compound was prepared from commercially available 4-chloro-5-methylthieno[2,3-d]pyrimidine and 1-(3-fluoro-4-hydroxyphenyl)-3-(2-(4-fluorophenyl)acetyl)thiourea (24 mg, 0.075 mmol, Compound A of Example 3). 1H NMR (CDCl3) δ 12.42 (s, 1H), 8.67 (s, 1H), 8.53 (s, 1H), 7.88 (dd, 1H, J=13.8, 2.2 Hz), 7.43 (s, 1H), 7.32 (m, 3 H), 7.09 (m, 3H), 3.72 (S, 2H), 2.67 (s, 3H); MS(ESI+) m/z 471 (M+H)+.

후처리

  1. customIn a similar manner as described for the preparation of Example 10

출처 및 근거

ORD 기록
ord-e0fc7d4e8a6942258b12470d07200790
출처 데이터셋
uspto-grants-2007_02
특허 번호
US07173031B2

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