Hydrazine → HCID 178513179、化合物
反応式
[ClH:1].Cl[C:3]1[CH:15]=[CH:14][C:6]([CH:7]=[N:8][NH:9][C:10](=[NH:13])SC)=[CH:5][CH:4]=1.[NH2:16][NH2:17]>C(O)C>[NH2:16][NH:17][C:10]([NH:9][NH:8][CH2:7][C:6]1[CH:14]=[CH:15][C:3]([Cl:1])=[CH:4][CH:5]=1)=[NH:13]参加物
4
実験手順
The same compound is synthesized by the reaction of equimolar quantities ofp-chlorobenzylhydrazine and methyl-3-(4-chlorobenzylidene)thiocarbazimidatehydrochloride (see Example 10) in hot ethanol. It is also prepared by the reaction of equimolar amounts of 1-(p-chlorobenzyl)-S-methylisothiosemicarbazide and hydrazine in warm ethanol, which affords 1-amino-3-(p-chlorobenzylamino)guanidine, followed by treatment of the latter with an equimolar quantity of p-chlorobenzaldehyde in hot isopropanol.
出典と根拠
- ORDレコード
- ord-38468505759c4437af74da3fe5444d5c
- 出典データセット
- uspto-grants-1976_11
- 特許番号
- US03992446
反応ノート
読み込み中…