Hydrochloric Acid → 6-[5-(2-Amino-ethoxy)-pyridin-3-yl]-7-fluoro-1-methyl-3,4-dihydro-1H-quinolin-2-one hydrochloride
反応式
C(OC(=O)[NH:7][CH2:8][CH2:9][O:10][C:11]1[CH:12]=[N:13][CH:14]=[C:15]([C:17]2[CH:18]=[C:19]3[C:24](=[CH:25][C:26]=2[F:27])[N:23]([CH3:28])[C:22](=[O:29])[CH2:21][CH2:20]3)[CH:16]=1)(C)(C)C.[ClH:31]>CO>[ClH:31].[NH2:7][CH2:8][CH2:9][O:10][C:11]1[CH:16]=[C:15]([C:17]2[CH:18]=[C:19]3[C:24](=[CH:25][C:26]=2[F:27])[N:23]([CH3:28])[C:22](=[O:29])[CH2:21][CH2:20]3)[CH:14]=[N:13][CH:12]=1参加物
4
反応物 2
生成物 1
試薬・触媒・溶媒 1
実験手順
In analogy to the procedure described for the preparation of example 42, reaction of {2-[5-(7-fluoro-1-methyl-2-oxo-1,2,3,4-tetrahydro-quinolin-6-yl)-pyridin-3-yloxy]-ethyl}-carbamic acid tert-butyl ester (example 232) with hydrogen chloride (in dixoane) in methanol gave the title compound as light yellow solid. MS: 316.5 (M+H+).
出典と根拠
- ORDレコード
- ord-bbf1b91ec28940e6a5467a824e012936
- 出典データセット
- uspto-grants-2016_02
- 特許番号
- US09260408B2
反応ノート
読み込み中…