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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 632389Generated: October 30, 2026

Hydrochloric Acid → 5-Cyclopropyl-6-((S)-3-hydroxy-1-trifluoromethyl-propoxy)-pyridine-2-carboxylic acid

https://huagongshe.com/reaction/632389

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1,3-Butanediol, 4,4,4-trifluoro-, (S)-HCID 10307869—
ReactantPotassium tert-butoxideHCID 23665647—
Reactant6-Chloro-5-cyclopropyl-2-pyridinecarboxylic acidHCID 86674793—
SolventDimethylformamideHCID 6228—
Product5-Cyclopropyl-6-((S)-3-hydroxy-1-trifluoromethyl-propoxy)-pyridine-2-carboxylic acidHCID 710872878.4%

Reaction Conditions

Temperature140 °C

Reaction Steps

6-Chloro-5-cyclopropyl-2-pyridinecarboxylic acid (CAN 1211530-95-8; 180 mg, 901 μmol), (S)-4,4,4-trifluorobutane-1,3-diol (394 mg, 2.73 mmol) and potassium tert-butoxide (307 mg, 2.73 mmol) were combined with DMF (3 mL) to give a white suspension. The reaction mixture was heated to 140° C. and stirred for 48 h. After cooling the mixture was poured into cold 1 M HCl (15 mL) and extracted with ethyl acetate (2×75 mL). The phases were combined, dried with Na2SO4 and concentrated in vacuo. The residue was purified by preparative HPLC to give the title compound (23 mg, 8.3%) and its regioisomer; MS (EI) 304.2 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09321727B2
Source datasetuspto-grants-2016_04
ORD IDord-dc3b23db98f44b85a5506e8995d656fc
Source noteuspto-grants-2016_04