Benzyloxyamine hydrochloride → HCID 53875714、化合物
反応式
[CH:1]1([N:6]2[C:14]3[C:9](=[CH:10][CH:11]=[C:12]([C:15]([NH:17][CH2:18][CH2:19][C:20](O)=[O:21])=[O:16])[CH:13]=3)[C:8]([CH2:23][CH3:24])=[N:7]2)[CH2:5][CH2:4][CH2:3][CH2:2]1.Cl.[CH2:26]([O:33][NH2:34])[C:27]1[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=1>>[CH2:26]([O:33][NH:34][C:20]([CH2:19][CH2:18][NH:17][C:15]([C:12]1[CH:13]=[C:14]2[C:9]([C:8]([CH2:23][CH3:24])=[N:7][N:6]2[CH:1]2[CH2:2][CH2:3][CH2:4][CH2:5]2)=[CH:10][CH:11]=1)=[O:16])=[O:21])[C:27]1[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=1参加物
3
実験手順
This compound was prepared according to the method of Example 37, using 250 mg (0.759 mmol, 1.0 equiv) 3-[(1-cyclopentyl-3-ethyl-1H-indazole-6-carbonyl)-amino]-propionic acid and 121 mg (0.759 mmol, 1.0 equiv) O-benzylhydroxylamine hydrochloride as starting materials, to give 237 mg (72%) of a white solid: mp 134-136° C.; Anal. calcd for C25H30N4O3: C, 69.10; H, 6.96; N, 12.89. Found: C, 69.36; H, 6.75; N, 12.85.
後処理
- customThis compound was prepared
出典と根拠
- ORDレコード
- ord-6c673c4fd184413db29d4fb3c5e8d4ae