Ethanol → Ethyl N-tert-butoxycarbonyl-4-(3-methane-sulfonylaminobenzyl)piperidine-4-carboxylate

反応式

[C:1]([CH3:2])([CH3:3])([CH3:4])[O:5][C:6](=[O:7])[N:8]1[CH2:9][CH2:10][C:11]([C:14](=[O:15])[O:16][CH2:17][CH3:18])([CH2:19][c:20]2[cH:21][c:22]([N+:26]([O-:27])=[O:28])[cH:23][cH:24][cH:25]2)[CH2:12][CH2:13]1.[CH3:29][S:30]([Cl:31])(=[O:32])=[O:33].[CH3:34][CH2:35][OH:36]>>[C:1]([CH3:2])([CH3:3])([CH3:4])[O:5][C:6](=[O:7])[N:8]1[CH2:9][CH2:10][C:11]([C:14](=[O:15])[O:16][CH2:17][CH3:18])([CH2:19][c:20]2[cH:21][c:22]([NH:26][S:30]([CH3:29])(=[O:32])=[O:33])[cH:23][cH:24][cH:25]2)[CH2:12][CH2:13]1

参加物

反応物 3

HCID 702Ethanol

HCID 31297Methanesulfonyl chloride

HCID 53931544ethyl N-tert-butoxycarbonyl-4-(3-nitrobenzyl)piperidine-4-carboxylate

生成物 1

HCID 21193321Ethyl N-tert-butoxycarbonyl-4-(3-methane-sulfonylaminobenzyl)piperidine-4-carboxylate

出典と根拠

ORDレコード: ord-b0a66842c9a049b2987b07317445fd68
出典データセット: Training data from https://doi.org/10.1039/C8SC04228D (1/10)
DOI: 10.1039/C8SC04228D

反応ノート

読み込み中…