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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1491868Generated: October 31, 2026

Formic Acid → HCID 9993589, compound

https://huagongshe.com/reaction/1491868

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormic AcidHCID 284—
ReactantAcetic AnhydrideHCID 7918—
ReactantTriethylamineHCID 8471—
Reactant4-(6-Aminomethylpyridin-2-yl)-2-(diaminomethyleneamino)thiazole trihydrochlorideHCID 18953837—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 9993589HCID 9993589—

Reaction Conditions

Temperature45 °C

Reaction Steps

A mixture of formic acid (0.47 ml) and acetic anhydride (0.87 ml) was stirred at 40-50° C. for 30 minutes. To a mixture of 4-(6-aminomethylpyridin-2-yl)-2(diaminomethyleneamino)thiazole trihydrochloride (3.0 g) and triethylamine (3.5 ml) in N,N-dimethylformamide (45 ml) was added the above mixture under ice-cooling and the mixture was stirred at ambient temperature for 5 hours. The reaction mixture was added to water and the mixture was extracted with a mixture of ethyl acetate and tetrahydrofuran. The extract layer was washed with brine, and dried over magnesium sulfate. Evaporation of a solvent gave a residue, which was purified by column chromatography on alumina, eluting with a mixture of chloroform and methanol (9:1, V/V). The eluted fractions containing the desired product were collected and evaporated in vacuo. The residue was recrystallized from an aqueous methanol to give 2-(diaminomethyleneamino)-4-(6-formylaminomethylpyridin-2-yl)thiazole (0.62 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05371097
Source datasetuspto-grants-1994_12
ORD IDord-1edf51dbf9224bce908cd868b240bb35
Source noteuspto-grants-1994_12