N,N-Dimethylethylenediamine → HCID 71542102、化合物

反応式

[C:1]12([C:11]3[CH:22]=[CH:21][C:14]([O:15][CH2:16][CH2:17][C:18]([OH:20])=O)=[CH:13][CH:12]=3)[CH2:10][CH:5]3[CH2:6][CH:7]([CH2:9][CH:3]([CH2:4]3)[CH2:2]1)[CH2:8]2.[CH3:23][N:24]([CH3:28])[CH2:25][CH2:26][NH2:27]>>[C:1]12([C:11]3[CH:12]=[CH:13][C:14]([O:15][CH2:16][CH2:17][C:18]([NH:27][CH2:26][CH2:25][N:24]([CH3:28])[CH3:23])=[O:20])=[CH:21][CH:22]=3)[CH2:8][CH:7]3[CH2:9][CH:3]([CH2:4][CH:5]([CH2:6]3)[CH2:10]1)[CH2:2]2

参加物

反応物 2

HCID 66053N,N-Dimethylethylenediamine

HCID 16772355(4-Adamantan-1-yl-phenoxymethyl)acetic acid

生成物 1

HCID 71542102HCID 71542102、化合物収率 92%

実験手順

The title compound was prepared from 3-(4-(adamantan-1-yl)phenoxy)propanoic acid (0.2 g, 0.66 mmol) and N,N-dimethylethane-1,2-diamine (0.058 g, 0.66 mmol) according to the example 1, which was given 3-(4-(adamantan-1-yl)phenoxy)-N-(2-(dimethylamino)ethyl)propanamide as a white solid (0.225 g, 91.4% yield).

出典と根拠

ORDレコード: ord-6164d71a03d244d4a4b5b2f972c057ea
出典データセット: uspto-grants-2016_04
DOI: 10.6084/m9.figshare.5104873.v1
特許番号: US09315507B2

反応ノート

読み込み中…

参加物