Tetrahydrofuran → HCID 11678456, 화합물
반응식
[NH2:1][C@@H:2]1[N:8]=[C:7]([C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)[C:6]2[CH:15]=[CH:16][CH:17]=[CH:18][C:5]=2[N:4]([CH2:19][C:20]([F:23])([F:22])[F:21])[C:3]1=[O:24].C(N(CC)CC)C.[OH:32][CH2:33][C:34]1[NH:35][C:36](=[O:45])[N:37]([CH:39]2[CH2:44][CH2:43][NH:42][CH2:41][CH2:40]2)[CH:38]=1.[O:46]1CCC[CH2:47]1>>[OH:32][CH2:33][C:34]1[NH:35][C:36](=[O:45])[N:37]([CH:39]2[CH2:44][CH2:43][N:42]([C:47]([NH:1][C@@H:2]3[N:8]=[C:7]([C:9]4[CH:10]=[CH:11][CH:12]=[CH:13][CH:14]=4)[C:6]4[CH:15]=[CH:16][CH:17]=[CH:18][C:5]=4[N:4]([CH2:19][C:20]([F:21])([F:23])[F:22])[C:3]3=[O:24])=[O:46])[CH2:41][CH2:40]2)[CH:38]=1참가 물질
실험 절차
(3R)-3-Amino-5-phenyl-1-(2,2,2-trifluoroethyl)-1,3-dihydro-2H-1,4-benzodiazepin-2-one (338 mg, 1.014 mmol) (Y.-J. Shi et al., Tetrahedron, 1999, 55, 909-918) and triethylamine (0.141 mL, 1.014 mmol) were added to a solution of p-nitrophenylchloroformate (204 mg, 1.014 mmol) in tetrahydrofuran (15 mL) at 0° C. After 1 h, 4-(hydroxymethyl)-1-piperidin-4-yl-1,3-dihydro-2H-imidazol-2-one (200 mg, 1.014 mmol) was added and the reaction stirred at 0 oC for 10 min and was then heated to 50 oC. After 4 h, the reaction was partitioned between ethyl acetate and saturated sodium bicarbonate and the organics were washed with water, brine, and dried over magnesium sulfate. Purification by preparative reverse phase chromatography gave the title compound (18 mg). MS 557.21 (M+1).
후처리
- temperaturewas then heated to 50 oC
- waitAfter 4 h
- customthe reaction was partitioned between ethyl acetate and saturated sodium bicarbonate
- washthe organics were washed with water, brine
- dry with materialdried over magnesium sulfate
- customPurification by preparative reverse phase chromatography
출처 및 근거
- ORD 기록
- ord-aa8d35887aa64b8294c52f927146610a
- 출처 데이터셋
- uspto-grants-2009_12
- 특허 번호
- US07632832B2
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