Water → 2-[3-(2-Cyanopyrrol-1-yl)benzoyl]guanidine

HRID 399877ノート

反応式

HRID 399877 の反応式
C[O-].[Na+].Cl.[NH2:5][C:6]([NH2:8])=[NH:7].[C:9]([C:11]1[N:12]([C:16]2[CH:17]=[C:18]([CH:23]=[CH:24][CH:25]=2)[C:19](OC)=[O:20])[CH:13]=[CH:14][CH:15]=1)#[N:10].O>CN(C)C=O>[C:9]([C:11]1[N:12]([C:16]2[CH:17]=[C:18]([CH:23]=[CH:24][CH:25]=2)[C:19]([N:7]=[C:6]([NH2:8])[NH2:5])=[O:20])[CH:13]=[CH:14][CH:15]=1)#[N:10]

参加物

6

反応物 4

HCID 962WaterHCID 5742Guanidine HydrochlorideHCID 10942334Sodium MethoxideHCID 18945318Methyl 3-(2-cyanopyrrol-1-yl)benzoate

生成物 1

HCID 189451892-[3-(2-Cyanopyrrol-1-yl)benzoyl]guanidine収率 63.4%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

28% Methanolic sodium methoxide (122.2 ml) was added to a solution of guanidine hydrochloride (63.7 g) in dry N,N-dimethylformamide (300 ml) and the mixture was stirred for 20 minutes at ambient temperature. To the mixture was added methyl 3-(2-cyanopyrrol-1-yl)benzoate (30.5 g), and the mixture was stirred for 2 hours at the same temperature. The reaction mixture was poured into water under stirring. The isolated precipitate was collected by filtration to give 2-[3-(2-cyanopyrrol-1-yl)benzoyl]guanidine (21.66 g).

後処理

  1. stirringthe mixture was stirred for 2 hours at the same temperature
  2. stirringunder stirring
  3. filtrationThe isolated precipitate was collected by filtration

出典と根拠

ORDレコード
ord-7103577844754c4eb7e2a352b01c9ad8
出典データセット
uspto-grants-1998_10
特許番号
US05824691

反応ノート

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