(3-Methylpyridin-4-yl)boronic acid → N,N-dibenzyl-5-(3-methyl-4-pyridinyl)-3,4-dihydro-2H-chromen-3-amine

反応式

[CH3:1][c:2]1[cH:3][n:4][cH:5][cH:6][c:7]1[B:8]([OH:9])[OH:10].[F:11][C:12]([F:13])([F:14])[S:15]([O:16][c:17]1[c:18]2[c:23]([cH:24][cH:25][cH:26]1)[O:22][CH2:21][CH:20]([N:27]([CH2:28][c:29]1[cH:30][cH:31][cH:32][cH:33][cH:34]1)[CH2:35][c:36]1[cH:37][cH:38][cH:39][cH:40][cH:41]1)[CH2:19]2)(=[O:42])=[O:43]>>[CH3:1][c:2]1[cH:3][n:4][cH:5][cH:6][c:7]1-[c:17]1[c:18]2[c:23]([cH:24][cH:25][cH:26]1)[O:22][CH2:21][CH:20]([N:27]([CH2:28][c:29]1[cH:30][cH:31][cH:32][cH:33][cH:34]1)[CH2:35][c:36]1[cH:37][cH:38][cH:39][cH:40][cH:41]1)[CH2:19]2

参加物

反応物 2

HCID 44754762(3-Methylpyridin-4-yl)boronic acid

HCID 74421935[3-(dibenzylamino)-3,4-dihydro-2H-chromen-5-yl] trifluoromethanesulfonate

生成物 1

HCID 140551734N,N-dibenzyl-5-(3-methyl-4-pyridinyl)-3,4-dihydro-2H-chromen-3-amine

出典と根拠

ORDレコード: ord-d3b6339fbd384a49867074e0baf42b54
出典データセット: Training data from https://doi.org/10.1039/C8SC04228D (5/10)
DOI: 10.1039/C8SC04228D

反応ノート

読み込み中…