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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 448135Generated: October 30, 2026

2,4,6-Trimethylpyridine → 5-tert-butyl 1-ethyl 3-[(4-chloromethyl-benzoyl)amino]-1H-thieno[2,3-c]pyrazole-1,5-dicarboxylate

https://huagongshe.com/reaction/448135

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4,6-TrimethylpyridineHCID 7953—
Reactant4-(Chloromethyl)benzoyl chlorideHCID 70136—
ReactantSodium BicarbonateHCID 516892—
Reactanttert-butyl 3-amino-1H-thieno[2,3-c]pyrazole-5-carboxylateHCID 178450636—
SolventDichloromethaneHCID 6344—
Product5-tert-butyl 1-ethyl 3-[(4-chloromethyl-benzoyl)amino]-1H-thieno[2,3-c]pyrazole-1,5-dicarboxylateHCID 66785832—

Reaction Conditions

Temperature20 °C

Reaction Steps

4-Chloromethylbenzoyl chloride (5.42 g 28.7 mmol) was added to a suspension of tert-butyl 3-amino-1H-thieno[2,3-c]pyrazole-5-carboxylate (5.94 g, 19.1 mmol) in dry DCM (150 mL) and 2,4,6-collidine (6.94 g, 57.3 mmol) under stirring at 20° C. The resulting suspension was stirred for 3 hours at room temperature. 300 mL of aqueous sodium bicarbonate were then added to the reaction mixture and the organic layer was separated, washed with brine, dried over sodium sulphate and evaporated. The residue was triturated with hexane, filtered and dried at 40° C. under vacuum to give 8.3 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481584B2
Source datasetuspto-grants-2013_07
ORD IDord-902743747b524328829a742c8cca5b3a
Source noteuspto-grants-2013_07