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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2298594Generated: October 25, 2026

Hydrazine hydrate (1:1) → N'-amino-5-methylsulfanyl-4-(4-phenyl-1,3-thiazol-2-yl)thiophene-2-carboximidamide

https://huagongshe.com/reaction/2298594

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine hydrate (1:1)HCID 24654—
Reactant5-Methylthio-4-(4-phenyl(1,3-thiazol-2-yl))thiophene-2-carbonitrileHCID 18537264—
SolventEthanolHCID 702—
ProductN'-amino-5-methylsulfanyl-4-(4-phenyl-1,3-thiazol-2-yl)thiophene-2-carboximidamideHCID 17850364145%

Reaction Steps

5-Methylthio-4-(4-phenyl(1,3-thiazol-2-yl))thiophene-2-carbonitrile (100 mg, 0.32 mmol) as prepared in previous step was dissolved in EtOH (10 mL). To this solution hydrazine monohydrate (10 eq) was added and the mixture was heated at reflux for 3 h. The EtOH solution was concentrated down to 1 mL and water (2 mL) was added to this solution. This resulted in the formation of a white solid. The solid was collected by filtration washed with a small amount of water and dried under vacuum to give 50 mg (45%) of hydrazino[5-methylthio-4-(4-phenyl(1,3-thiazol-2-yl))(2-thienyl)]methanimine. 1H-NMR (CD3OD/CDCl3; 300 MHz) δ2.69 (s, 3H), 7.35-7.43 (m, 1H), 7.44-7.49 (m, 2H), 7.52 (s, 1H), 7.96-7.99 (m, 2), 8.10 (s, 1H). Mass spectrum (ESI, m/z): Calcd. for C15H14N4S3, 347.04 (M+H), found 347.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06492403B1
Source datasetuspto-grants-2002_12
ORD IDord-e66313bc1edc41408ca961bb42437c08
Source noteuspto-grants-2002_12