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HRID 38133作成日:2026年10月25日

Hydrazine, dihydrochloride → HCID 178428372、化合物

https://huagongshe.com/reaction/38133

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrazine, dihydrochlorideHCID 17548—
反応物(5-Chloro(2-thienyl))-n-({[4-(5-chloro-1,3-dioxobenzo[c]azolin-2-yl)-3-methylphenyl]amino}thioxomethyl)carboxamideHCID 20800070—
溶媒DimethylformamideHCID 6228—
生成物HCID 178428372HCID 17842837214.2%

反応手順

To a suspension of (5-chloro(2-thienyl))-N-({[4-(5-chloro-1,3-dioxobenzo[c]azolin-2-yl)-3-methylphenyl]amino}thioxomethyl)carboxamide (15 mg, 0.030 mmol) and hydrazine dihydrochloride (4 mg, 0.038 mmol) in DMF (0.3 mL) was added HgO (7 mg, 0.032 mmol). The reaction was stirred at room temp for 17 hr, and HPLC purified to give the desired product 5-chloro-2-(4-{[5-(5-chloro(2-thienyl))(4H-1,2,4-triazol-3-yl)]amino}-2-methylphenyl)benzo[c]azoline-1,3-dione (2 mg) (ES-MS (M+H)+=470, 472) and the aminoguanidine intermediate N-((1E)-2-aza-1-{[4-(5-chloro-1,3-dioxobenzo[c]azolidin-2-yl)-3-methylphenyl]amino}-2-aminovinyl)(5-chloro(2-thienyl))carboxamide (2 mg) ES-MS (M+H)+=488, 490 (2Cl).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08524721B2
出典データセットuspto-grants-2013_09
ORD IDord-3dbd1661402841ceb13eab318ed44ef4
出典メモuspto-grants-2013_09