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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 585497Generated: October 25, 2026

Trifluoroacetic acid → 3-Methyl-2-(2-phenyl-6,7-dihydro-4H-thiazolo[5,4-c]pyridine-5-sulfonylmethyl)-butyric Acid

https://huagongshe.com/reaction/585497

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTriethylamineHCID 8471—
Reactant2-Chlorosulfonylmethyl-3-methyl-butyric acid tert-butyl esterHCID 21259094—
Reactant2-phenyl-4H,5H,6H,7H-(1,3)thiazolo(5,4-c)pyridineHCID 22337487—
SolventDichloromethaneHCID 6344—
Product3-Methyl-2-(2-phenyl-6,7-dihydro-4H-thiazolo[5,4-c]pyridine-5-sulfonylmethyl)-butyric AcidHCID 2233749074.8%

Reaction Steps

2-Phenyl-4,5,6,7-tetrahydro-thiazolo[5,4-c]pyridine (0.11 g) was added to a solution of 2-chlorosulfonylmethyl-3-methyl-butyric acid tert-butyl ester (0.14 g) and triethylamine (0.3 ml) in DCM (20 ml) at room temperature. The solution was stirred for 2 h, then TFA (5 ml) was added and the mixture stirred for 1 h. The mixture was evaporated in vacuo and the residue partitioned between diethyl ether (10 ml) and saturated sodium bicarbonate (30 ml). The aqueous layer was acidified with citric acid to pH 5 and extracted with ethyl acetate (3×20 ml). The solvent was dried (MgSO4) and evaporated to give the title compound as pale yellow solid (0.15 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06933306B2
Source datasetuspto-grants-2005_08
ORD IDord-2339fe50dba34ccb9bc4f0fdebe3e84b
Source noteuspto-grants-2005_08