Sodium borohydride → (S)-N-((S)-1-Amino-3-(4-hydroxyphenyl)-1-oxopropan-2-yl)-2-((S)-2-(2-(5-(hydroxymethyl)thiazol-2-ylamino)acetamido)propanamido)propanamide
반응식
[NH2:1][C:2](=[O:34])[C@@H:3]([NH:12][C:13](=[O:33])[C@@H:14]([NH:16][C:17](=[O:32])[C@@H:18]([NH:20][C:21](=[O:31])[CH2:22][NH:23][C:24]1[S:25][C:26]([CH:29]=[O:30])=[CH:27][N:28]=1)[CH3:19])[CH3:15])[CH2:4][C:5]1[CH:10]=[CH:9][C:8]([OH:11])=[CH:7][CH:6]=1.[BH4-].[Na+]>CCO.O>[NH2:1][C:2](=[O:34])[C@@H:3]([NH:12][C:13](=[O:33])[C@@H:14]([NH:16][C:17](=[O:32])[C@@H:18]([NH:20][C:21](=[O:31])[CH2:22][NH:23][C:24]1[S:25][C:26]([CH2:29][OH:30])=[CH:27][N:28]=1)[CH3:19])[CH3:15])[CH2:4][C:5]1[CH:6]=[CH:7][C:8]([OH:11])=[CH:9][CH:10]=1참가 물질
4
반응물 2
생성물 1
시약·촉매·용매 1
실험 절차
To a suspension of material from Example 7 (13.2 mg, 0.022 mmol) in EtOH/H2O (4:1) (1.5 mL) is added solid sodium borohydride (7.8 mg, 0.206 mmol) in 2 equal portions over 1 b. After the addition is complete, the reaction is stirred at room temp for 1.5 h and evaporated to dryness to give the title compound (quantitative yield) as a white solid that is used crude in the next step. LC/MS (Condition A): ret. T=0.94-1.16 min, (M+Na) 515.
후처리
- additionAfter the addition
- customevaporated to dryness
출처 및 근거
- ORD 기록
- ord-7b52fcdd6e5a4c97a6f7db490f62860a
- 출처 데이터셋
- uspto-grants-2015_10
- 특허 번호
- US09169295B2
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