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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1904287Generated: November 2, 2026

Water → N-(1,1-dimethyl-4-indanyl)-2-chloro-4-methylthiazole-5-carboxamide

https://huagongshe.com/reaction/1904287

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPyridineHCID 1049—
Reactant1,1-Dimethyl-2,3-dihydro-1H-inden-4-amineHCID 13115615—
Reactant2-Chloro-4-methylthiazole-5-carboxylic acid chlorideHCID 13593393—
SolventTetrahydrofuranHCID 8028—
ProductN-(1,1-dimethyl-4-indanyl)-2-chloro-4-methylthiazole-5-carboxamideHCID 1453576193%

Reaction Steps

To a solution of 0.82 g (5.07 mmol) of 1,1-dimethyl-4-aminoindan and 0.48 g (6.08 mmol) of pyridine in 10 ml of tetrahydrofuran was added dropwise with stirring below 5° C. under ice cooling, a solution of 0.99 g (5.07 mmol) of 2-chloro-4-methylthiazole-5-carboxylic acid chloride in 3 ml of tetrahydrofuran, followed by stirring at room temperature overnight. The reaction mixture was poured into water and extracted with ethyl acetate. The organic layer was washed with 5% hydrochloric acid and then water and was dried over anhydrous sodium sulfate. The solvent was distilled off to obtain crystals, which was washed with n-hexane and dried to obtain 1.51 g of N-(1,1-dimethyl-4-indanyl)-2-chloro-4-methylthiazole-5-carboxamide (yeild 93%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04837242
Source datasetuspto-grants-1989_06
ORD IDord-cbb78989544144cab9e54c73d9219a5f
Source noteuspto-grants-1989_06