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[CH3:1][O:2][C:3]1[CH:12]=[CH:11][CH:10]=[C:9]2[C:4]=1[CH2:5][CH2:6][CH:7]([NH:13][CH2:14][CH2:15][CH3:16])[CH2:8]2.C(N(CC)CC)C.[Cl:24][CH2:25][C:26](Cl)=[O:27]>>[Cl:24][CH2:25][C:26]([N:13]([CH:7]1[CH2:6][CH2:5][C:4]2[C:9](=[CH:10][CH:11]=[CH:12][C:3]=2[O:2][CH3:1])[CH2:8]1)[CH2:14][CH2:15][CH3:16])=[O:27]참가 물질
4
실험 절차
This compound was prepared from 32b (4.63 g, 21.1 mmol), triethyl amine (5.1 ml, 42.2 mmol), and chloroacetyl chloride (1.80 ml, 25.4 mmol) by following Procedure B to give 33b (5.8 g, 93%). 1H NMR (400 MHz, CDCl3) 0.90-0.98 (m, 3H), 1.64-1.72 (m, 2H), 3.19-3.27 (m, 2H), 4.00 (s, 3H), 6.61-6.68 (m, 2H), 6.96-7.04 (m, 1H).
출처 및 근거
- ORD 기록
- ord-52d4e3cc2c97418bac088f3b57b7a4cb
- 출처 데이터셋
- uspto-grants-2015_05
- 특허 번호
- US09034877B2
연결된 노트
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