Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1708942Generated: November 3, 2026

Hydrochloric Acid → HCID 178522473, compound

https://huagongshe.com/reaction/1708942

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDimethylformamideHCID 6228—
ReactantThionyl ChlorideHCID 24386—
Reactant4-Amino-2-(3-pyridyl)thiazoleHCID 14772715—
ReactantHCID 178524966HCID 178524966—
SolventBenzeneHCID 241—
SolventWaterHCID 962—
SolventPyridineHCID 1049—
SolventAcetonitrileHCID 6342—
ProductHCID 178522473HCID 17852247338%

Reaction Steps

A mixture, obtained oy adding dry DMF (0.197 ml, 2.63 mmol) and then thionyl chloride (0.192 ml, 2.63 mmol) to dry benzene (1 ml) under ice-cooling, was allowed to warm up to room temperature and to react for 10 minutes upon which the mixture separated into two layers. The lower layer was added dropwise to dipotassium salt of 1H-tetrazole-5-carboxylic acid (333 mg, 1.75 mmol) suspended in dry acetonitrile (5 ml) under ice-cooling. The mixture was allowed to react for 15 minutes. After adding dropwise a mixed solution of 2-(3-pyridyl)4-thiazolamine (330 mg, 1.86 mmol) in dry acetonitrile (3 ml) and dry pyridine (1 ml) under the same conditions, the mixture was allowed to warm up to room temperature and to react for 1 hour. After dissolution was effected with addition of water, the reaction mixture was neutralized under ice-cooling with 2N-HCl to pH 7. The deposited solids were filtered with suction, was recrystallized from methanol-THF-water to give yellow crystals (181 mg, yield 38%) of N-(2-(3-pyridyl)-4-thiazolyl)-1H-tetrazole-5-carboxamide (Ia-23), m.p. 263°-265° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04946855
Source datasetuspto-grants-1990_08
ORD IDord-36a33e99e31e46b58cef4ccdea5e6bea
Source noteuspto-grants-1990_08