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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 659682Generated: October 30, 2026

Citric Acid → HCID 67132957, compound

https://huagongshe.com/reaction/659682

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCitric AcidHCID 311—
ReactantBoron TrichlorideHCID 25135—
ReactantButyl chloroformateHCID 61140—
Reactant2-(Pyrrolidin-1-yl)pyridineHCID 11019020—
ReactantHCID 67133271HCID 67133271—
SolventDichloromethaneHCID 6344—
ProductHCID 67132957HCID 6713295788%

Reaction Steps

To a solution of 3-[3-(3-trifluoromethylpyrazol-1-ylmethyl)phenyl]-5-iso-butyl-N-tert-butylthiophene-2-sulfonamide (43.5 mg, 0.087 mmol; see step (a)) in CH2Cl2 (2 mL) was added BCl3 (0.6 mL, 1.0 M in hexane) and the reaction mixture was stirred for 1 h at ambient temperature. The reaction mixture was concentrated in vacuo. Water (5 mL) was added to the residue and this was then extracted with EtOAc. The combined organic phase was washed with water and brine, dried (over anhydrous MgSO4) and concentrated in vacuo. To the crude product dissolved in pyridine (1.5 mL) was added pyrrolidinopyridine (25.8 mg, 0.174 mmol) and butyl chloroformate (110.7 μL, 0.87 mmol) and the reaction mixture was stirred overnight. Citric acid (3 mL, 10% aq) was added to the reaction mixture, which was then extracted with EtOAc, dried (over anhydrous MgSO4), concentrated in vacuo, and the residue purified by LCMS (40-100% CH3CN in water) to give the title compound in 88% yield, over two steps, (41.6 mg, 0.076 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08080571B2
Source datasetuspto-grants-2011_12
ORD IDord-ead5723a941c422281970783a9ad1ea9
Source noteuspto-grants-2011_12