Triethylamine → HCID 19761271、化合物
反応式
[ClH:1].[NH:2]1[CH2:7][CH2:6][CH:5]([N:8]([CH3:19])[C:9](=[O:18])[O:10][CH2:11][C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)[CH2:4][CH2:3]1.I[CH2:21][CH:22]1[C:25]2=[CH:26][CH:27]=[CH:28][CH:29]=[C:24]2[CH2:23]1.[CH2:30](N(CC)CC)C>>[ClH:1].[C:22]1([CH2:21][N:2]2[CH2:3][CH2:4][CH:5]([N:8]([CH2:19][CH3:30])[C:9](=[O:18])[O:10][CH2:11][C:12]3[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=3)[CH2:6][CH2:7]2)[C:25]2[CH:26]=[CH:27][CH:28]=[CH:29][C:24]=2[CH:23]=1参加物
4
実験手順
Benzyl N-[1-(benzocyclobuten-1-ylmethyl)-piperid-4-yl]-N-ethylcarbamate hydrochloride was prepared from benzyl N-piperid-4-yl-N-methylcarbamate hydrochloride and 1-iodomethylbenzocyclobutene, in accordance with the process described in Stage C of Example 8, in the presence of triethylamine.
出典と根拠
- ORDレコード
- ord-3f0cbc700de241c99ac6a908da39fee6