Isopropyl isocyanate → HCID 68628895、化合物

反応式

Cl[C:2]1[CH:11]=[CH:10][C:9]2[C:4](=[CH:5][CH:6]=[C:7]([N+:12]([O-])=O)[CH:8]=2)[N:3]=1.[CH3:15][CH:16]1[CH2:20][C:19]2[CH:21]=[CH:22][CH:23]=[C:24]([NH2:25])[C:18]=2[O:17]1.[CH:26]([N:29]=[C:30]=[O:31])([CH3:28])[CH3:27]>>[CH:26]([NH:29][C:30]([NH:12][C:7]1[CH:8]=[C:9]2[C:4](=[CH:5][CH:6]=1)[N:3]=[C:2]([NH:25][C:24]1[C:18]3[O:17][CH:16]([CH3:15])[CH2:20][C:19]=3[CH:21]=[CH:22][CH:23]=1)[CH:11]=[CH:10]2)=[O:31])([CH3:28])[CH3:27]

参加物

反応物 3

HCID 61277Isopropyl isocyanate

HCID 109217232-Chloro-6-nitroquinoline

HCID 135358262-Methyl-2,3-dihydrobenzofuran-7-amine

生成物 1

HCID 68628895HCID 68628895、化合物

実験手順

The title compound, MS: m/e=377.4 (M+H+), was prepared in accordance with the general method of example 14 from 2-chloro-6-nitro-quinoline, 2,3-dihydro-2-methyl-7-benzofuranamine (CAS 26210-74-2) and isopropyl isocyanate.

出典と根拠

ORDレコード: ord-6f7e4f5a505d430b93e5db368dae9c39
出典データセット: uspto-grants-2013_01
DOI: 10.6084/m9.figshare.5104873.v1
特許番号: US08350028B2

反応ノート

読み込み中…