Benzenemethanamine, 3-chloro- → N-(3-chlorobenzyl)-N'-(3-methyl-5-isoquinolinyl)urea

HRID 2056896ノート

反応式

HRID 2056896 の反応式
[Cl:1][C:2]1[CH:3]=[C:4]([CH:7]=[CH:8][CH:9]=1)[CH2:5][NH2:6].[N:10]([C:13]1[CH:22]=[CH:21][CH:20]=[C:19]2[C:14]=1[CH:15]=[C:16]([CH3:23])[N:17]=[CH:18]2)=[C:11]=[O:12]>CCOCC>[Cl:1][C:2]1[CH:3]=[C:4]([CH:7]=[CH:8][CH:9]=1)[CH2:5][NH:6][C:11]([NH:10][C:13]1[CH:22]=[CH:21][CH:20]=[C:19]2[C:14]=1[CH:15]=[C:16]([CH3:23])[N:17]=[CH:18]2)=[O:12]

参加物

4

反応物 2

HCID 77802Benzenemethanamine, 3-chloro-HCID 222283825-Isocyanato-3-methylisoquinoline

生成物 1

HCID 22032619N-(3-chlorobenzyl)-N'-(3-methyl-5-isoquinolinyl)urea

試薬・触媒・溶媒 1

HCID 3283Diethyl Ether溶媒

実験手順

3-chlorobenzylamine (141 mg, 1.0 mmol) in ether (20 mL) was treated with an ethereal solution of 5-isocyanato-3-methylisoquinoline. The precipitate that formed was collected by filtration, washed with diethyl ether, and air-dried to provide the title compound. 1H NMR (300 MHz, DMSO-d6) δ 9.18 (s, 1H), 8.69 (s, 1H), 8.20 (d, 1H, J=7.8 Hz), 7.75 (s, 1H), 7.70 (d, 1H, J=8.2 Hz), 7.51 (t, 1H, J=7.8 Hz), 7.31-7.43 (m, 4H), 7.10 (m, 1H), 4.38 (d, 2H, J=5.7 Hz), 2.65 (s, 3H); MS (ESI+) m/z 326/328 (M+H, 35Cl/37Cl).

後処理

  1. customThe precipitate that formed
  2. filtrationwas collected by filtration
  3. washwashed with diethyl ether
  4. customair-dried

出典と根拠

ORDレコード
ord-13a4d54d16744c978b7cfd15937997bb
出典データセット
uspto-grants-2008_02
特許番号
US07335678B2

反応ノート

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