Isopropylamine → HCID 42641986, 화합물

HRID 1715582노트

반응식

HRID 1715582 반응식
CS(OS(C)(=O)=O)(=O)=O.[C:10]([C:14]1[CH:15]=[C:16]([NH:20][C:21]([NH:23][CH2:24][C:25]2[CH:30]=[CH:29][CH:28]=[CH:27][C:26]=2[NH:31][C:32]2[CH:33]=[C:34]3[C:38](=[CH:39][CH:40]=2)[N:37]([CH2:41][CH2:42][CH2:43]O)[N:36]=[CH:35]3)=O)[N:17]([CH3:19])[N:18]=1)([CH3:13])([CH3:12])[CH3:11].[CH:45]([N:48](C(C)C)CC)([CH3:47])[CH3:46].C(N)(C)C.CC#N.[OH2:61]>>[C:10]([C:14]1[CH:15]=[C:16]([NH:20][C:21]([NH:23][CH2:24][C:25]2[CH:30]=[CH:29][CH:28]=[CH:27][C:26]=2[NH:31][C:32]2[CH:33]=[C:34]3[C:38](=[CH:39][CH:40]=2)[N:37]([CH2:41][CH2:42][CH2:43][NH:48][CH:45]([CH3:47])[CH3:46])[N:36]=[CH:35]3)=[O:61])[N:17]([CH3:19])[N:18]=1)([CH3:13])([CH3:12])[CH3:11]

참가 물질

6

실험 절차

Methanesulfonic anhydride (18 mg, 0.11 mmol) was added to a solution of alcohol (7s) (36 mg, 0.076 mmol) and diisopropylethylamine (29 mg, 0.23 mmol) at room temperature. The solution was stirred for 1 hour. Isopropylamine (0.13 mL, 1.50 mmol) was added and the reaction was stirred at room temperature for 60 hours. The volatiles were removed in vacuo. The crude product was purified on silica gel with 5% MeOH/CH2Cl2 containing 1% Et3N and then on C18 silica with CH3CN/H2O to afford the desired compound (8s-2) (8 mg, 20% yield). 1HNMR (400 MHz, MeOD) δ 7.88 (s, 1H), 7.51 (d, J=8.6 Hz, 1H), 7.31-7.24 (m, 3H), 7.17-7.16 (m, 2H), 6.93-6.89 (m, 1H), 6.05 (s, 1H), 4.52 (t, J=10.2 Hz, 2H), 4.41 (s, 2H), 3.57 (s, 3H), 3.35-3.30 (m, 1H), 3.03 (t, J=11.7 Hz, 2H), 2.29-2.22 (m, 2H), 1.29 (d, J=6.3 Hz, 6H), 1.26 (s, 9H); MS (ESI+) m/z 517 (M+H)+; HPLC (5 to 95%) 2.61 min.

후처리

  1. stirringthe reaction was stirred at room temperature for 60 hours
  2. customThe volatiles were removed in vacuo
  3. customThe crude product was purified on silica gel with 5% MeOH/CH2Cl2 containing 1% Et3N

출처 및 근거

ORD 기록
ord-ac4e9056c92747c8b826531abef6827e
출처 데이터셋
uspto-grants-2010_09
특허 번호
US07799782B2

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