3-(Trifluoromethyl)pyrrolidin-3-ol hydrochloride → HCID 90204148、化合物
反応式
[CH:1]1([C:4]2[CH:5]=[CH:6][C:7]([C:15]([OH:17])=O)=[N:8][C:9]=2[O:10][CH2:11][CH:12]2[CH2:14][CH2:13]2)[CH2:3][CH2:2]1.Cl.[F:19][C:20]([F:28])([F:27])[C:21]1([OH:26])[CH2:25][CH2:24][NH:23][CH2:22]1>>[CH:1]1([C:4]2[CH:5]=[CH:6][C:7]([C:15]([N:23]3[CH2:24][CH2:25][C:21]([OH:26])([C:20]([F:28])([F:27])[F:19])[CH2:22]3)=[O:17])=[N:8][C:9]=2[O:10][CH2:11][CH:12]2[CH2:13][CH2:14]2)[CH2:2][CH2:3]1参加物
3
実験手順
In analogy to the procedure described in Example 127 e), 5-cyclopropyl-6-cyclopropylmethoxy-pyridine-2-carboxylic acid (Example 3 c, 20 mg, 85.7 μmol) was reacted with 3-(trifluoromethyl)pyrrolidin-3-ol hydrochloride (CAN 1334147-81-7, 19.7 mg, 103 μmol) to obtain the title compound (15 mg, 47%) as colorless liquid, MS (EI): m/e=371.3 [MH+].
出典と根拠
- ORDレコード
- ord-2b534ef3fc914ed59aec0833a758665c
- 出典データセット
- uspto-grants-2016_04