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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2379857Generated: November 4, 2026

Triethylamine → 2-(Diaminomethyleneamino)-4-[2-(furfurylthio)acetylaminomethylthiazol-4-yl]thiazole

https://huagongshe.com/reaction/2379857

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant(Furfurylthio)acetic acidHCID 3021476—
Reactant4-(2-Aminomethylthiazol-4-yl)-2-(diaminomethyleneamino)thiazole dihydrochlorideHCID 18953834—
SolventDimethylformamideHCID 6228—
Product2-(Diaminomethyleneamino)-4-[2-(furfurylthio)acetylaminomethylthiazol-4-yl]thiazoleHCID 1895385611%

Reaction Steps

A suspension of 4-(2-aminomethylthiazol-4-yl)-2-(diaminomethyleneamino)thiazole dihydrochloride (1.6 g), (furfurylthio)acetic acid (0.98 g), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (1.2 g) and triethylamine (1.0 g) in N,N-dimethylformamide (20 ml) was stirred with cooling on an ice-water bath for 2.5 hours. The solvent was removed under the reduced pressure. The residue was washed with water and then chromatographed on a silica gel column eluting with a mixture of chloroform and methanol (10:1). The appropriate fractions was collected and the solvent was removed under the reduced pressure. The residue was suspended in water (20 ml) and the mixture was alkalized to pH 11 with a saturated aqueous potassium carbonate solution. The resulting precipitate was collected by filtration. Recrystallization from a mixture of methanol and water afforded 2-(diaminomethyleneamino)-4-[2-(furfurylthio)acetylaminomethylthiazol-4-yl]thiazole (0.22 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05364871
Source datasetuspto-grants-1994_11
ORD IDord-f2a30af2b464421baa6da69ffc5a7a5b
Source noteuspto-grants-1994_11