반응식
[C:1](Cl)(Cl)=[S:2].[NH2:5][C:6]1[C:15]2[C:10](=[C:11]([O:18][CH3:19])[CH:12]=[C:13]([O:16][CH3:17])[CH:14]=2)[C:9]([CH2:20][N:21]2[C:29](=[O:30])[C:28]3[C:23](=[CH:24][CH:25]=[CH:26][CH:27]=3)[C:22]2=[O:31])=[N:8][CH:7]=1.C[CH2:33][N:34](C(C)C)C(C)C.N.BrC[C:44](=O)[C:45]([OH:47])=[O:46]>C1COCC1>[O:31]=[C:22]1[C:23]2[C:28](=[CH:27][CH:26]=[CH:25][CH:24]=2)[C:29](=[O:30])[N:21]1[CH2:20][C:9]1[C:10]2[C:15](=[CH:14][C:13]([O:16][CH3:17])=[CH:12][C:11]=2[O:18][CH3:19])[C:6]([NH:5][C:33]2[S:2][CH:1]=[C:44]([C:45]([OH:47])=[O:46])[N:34]=2)=[CH:7][N:8]=1참가 물질
7
반응물 5
생성물 1
시약·촉매·용매 1
실험 절차
Thiophosgene (146 μL, 1.92 mmol) was added to a solution of Example 45C (580 mg, 1.6 mmol) and DIEA (670 μL) in THF (10 mL). After stirring for 1 h, the reaction was poured over aqueous ammonia and extracted with EtOAc. Organics were dried (MgSO4) and concentrated. The resulting crude thiourea was dissolved in THF (5 mL). Bromopyruvic acid (320 mg, 1.92 mmol) was added, and the reaction stirred for 2 h. Purification by silica gel chromatography (10% MeOH/CHCl3) gave 590 mg (75%) of the title compound as a tan solid. H1-NMR (MeOD-d4): δ 9.95 (br s, 1H), 8.81 (br s, 1H), 7.87-7.96 (m, 4H), 7.60 (br s, 1H), 7.14 (s, 1H), 6.86 (s, 1H), 5.41 (s, 2H), 4.09 (s, 3H), 3.94 (s, 3H). MS (ES) (M+H) calc'd for C24H18N4O6S, 491; found 491.
후처리
- extractionextracted with EtOAc
- dry with materialOrganics were dried (MgSO4)
- concentrationconcentrated
- dissolutionThe resulting crude thiourea was dissolved in THF (5 mL)
- stirringthe reaction stirred for 2 h
- customPurification by silica gel chromatography (10% MeOH/CHCl3)
출처 및 근거
- ORD 기록
- ord-aac9a72a39a84e959ebd805c61d91840
- 출처 데이터셋
- uspto-grants-2010_06
- 특허 번호
- US07732446B1
연결된 노트
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