Nitromethane → HCID 54347464、化合物

HRID 845243ノート

反応式

HRID 845243 の反応式
[CH2:1]([O:3][C:4]([C:6]1[N:7]=[CH:8][C:9]2[NH:10][C:11]3[C:16]([C:17]=2[C:18]=1[CH3:19])=[C:15]([CH:20]=O)[CH:14]=[CH:13][CH:12]=3)=[O:5])[CH3:2].[N+:22]([CH3:25])([O-:24])=[O:23].Cl.CN.C(=O)([O-])[O-].[Na+].[Na+]>C(O)C>[CH2:1]([O:3][C:4]([C:6]1[N:7]=[CH:8][C:9]2[NH:10][C:11]3[C:16]([C:17]=2[C:18]=1[CH3:19])=[C:15]([CH:20]=[CH:25][N+:22]([O-:24])=[O:23])[CH:14]=[CH:13][CH:12]=3)=[O:5])[CH3:2]

参加物

6

実験手順

A solution of 5-formyl-4-methyl-beta-carboline-3-carboxylic acid ethyl ester (10 g), nitromethane (2 ml) and methylamine hydrochloride (0.2 g) in ethanol (50 ml) is mixed with sodium carbonate (0.3 g) and left for 5 days at 20° C. with occasional shaking. Then it is evaporated to beginning crystallization. 5 g of the title compound crystallizes from the solution cooled with ice water.

後処理

  1. customThen it is evaporated
  2. customcrystallization
  3. custom5 g of the title compound crystallizes from the solution
  4. temperaturecooled with ice water

出典と根拠

ORDレコード
ord-5adfe4539b964b9f8851823f8deb2598
出典データセット
uspto-grants-1988_07
特許番号
US04757070

反応ノート

読み込み中…