Piperidine → 5-(t-Butoxycarbonylamino)-3-(8-hydroxyquinol-5-ylmethylen)-2-oxindole

反応式

[C:1]([CH3:2])([CH3:3])([CH3:4])[O:5][C:6](=[O:7])[NH:8][c:9]1[cH:10][c:11]2[c:15]([cH:16][cH:17]1)[NH:14][C:13](=[O:18])[CH2:12]2.[CH2:32]1[CH2:33][CH2:34][NH:35][CH2:36][CH2:37]1.[OH:19][c:20]1[cH:21][cH:22][c:23]([CH:30]=[O:31])[c:24]2[cH:25][cH:26][cH:27][n:28][c:29]12>>[C:1]([CH3:2])([CH3:3])([CH3:4])[O:5][C:6](=[O:7])[NH:8][c:9]1[cH:10][c:11]2[c:15]([cH:16][cH:17]1)[NH:14][C:13](=[O:18])[C:12]2=[CH:30][c:23]1[cH:22][cH:21][c:20]([OH:19])[c:29]2[c:24]1[cH:25][cH:26][cH:27][n:28]2

参加物

反応物 3

HCID 8082Piperidine

HCID 2753638-Hydroxyquinoline-5-carbaldehyde

HCID 53971753tert-Butyl (2-oxoindolin-5-yl)carbamate

生成物 1

HCID 676013225-(t-Butoxycarbonylamino)-3-(8-hydroxyquinol-5-ylmethylen)-2-oxindole

出典と根拠

ORDレコード: ord-b85a5282c9b34767955e74b896c52537
出典データセット: Training data from https://doi.org/10.1039/C8SC04228D (3/10)
DOI: 10.1039/C8SC04228D

反応ノート

読み込み中…