5-Methylthiophene-2-carbohydrazide → 5-Methyl-thiophen-2-carboxylic acid (1-amino-2-benzenesulfonyl-ethylidene)-hydrazide

HRID 277030

反応式

C(O[C:4](=[NH:15])[CH2:5][S:6]([C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1)(=[O:8])=[O:7])C.[CH3:16][C:17]1[S:21][C:20]([C:22]([NH:24][NH2:25])=[O:23])=[CH:19][CH:18]=1>C(Cl)(Cl)Cl>[NH2:15][C:4](=[N:25][NH:24][C:22]([C:20]1[S:21][C:17]([CH3:16])=[CH:18][CH:19]=1)=[O:23])[CH2:5][S:6]([C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1)(=[O:8])=[O:7]

参加物

実験手順

1.75 g (0.0077 Mol) of 2-(phenylsulfonyl)-ethanimidic acid ethyl ester was stirred together with 1.2 g (0.0077 mol) 5-methyl-thiophen-2-carboxylic acid hydrazide in 14 ml chloroform for 24 hours at 50° C. The resulting precipitate was filtered off and dried. 2.37 g of 5-methyl-thiophen-2-carboxylic acid (1-amino-2-benzenesulfonyl-ethylidene)-hydrazide was obtained as off-white crystals. Mp.: 222° C. (dec.).

後処理

filtrationThe resulting precipitate was filtered off
customdried

出典と根拠

ORDレコード: ord-320543ae4d58441c90f95b881d746d71
出典データセット: uspto-grants-2002_03
DOI: 10.6084/m9.figshare.5104873.v1
特許番号: US06355653B1

反応式

参加物

反応物 2

生成物 1

試薬・触媒・溶媒 1

実験手順

後処理

出典と根拠

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