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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1708941Generated: November 1, 2026

Hydrochloric Acid → HCID 178423991, compound

https://huagongshe.com/reaction/1708941

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDimethylformamideHCID 6228—
ReactantThionyl ChlorideHCID 24386—
Reactant2-(4-Methylphenyl)-4-thiazolamineHCID 14772702—
ReactantHCID 178524966HCID 178524966—
SolventBenzeneHCID 241—
SolventWaterHCID 962—
SolventPyridineHCID 1049—
SolventAcetonitrileHCID 6342—
ProductHCID 178423991HCID 17842399152%

Reaction Steps

A mixture, obtained by adding ice-cooled dry DMF(0.53 ml, 6.48 mmol) and then thionyl chloride (0.499 ml, 6.84 mmol) to dry benzene (1.5 ml,, 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 (867 mg, 4.56 mmol) suspended in dry acetonitrile (15 ml) under ice-cooling. The mixture was allowed to react for 15 minutes. After adding dropwise a mixed solution of 2-(4-methylphenyl)-4-thiazolamine (928 mg, 4.88 mmol) in dry acetonitrile (15 ml) and dry pyridine (4 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 acidified under ice-cooling with 2N-HCl to pH 2. The deposited solids were filtered with suction, washed with water and recrystallized from methanol-water to give yellowish crystals (677 mg. yield 52%) of N-(2-(4-methylphenyl)-4-thiazolyl)-1H-tetrazole-5-carboxamide (Ia-5), m.p.228°-230° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04946855
Source datasetuspto-grants-1990_08
ORD IDord-b19f4e1c0a1441768b389cf072ca1ec9
Source noteuspto-grants-1990_08