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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 659678Generated: October 30, 2026

Citric Acid → HCID 67133104, compound

https://huagongshe.com/reaction/659678

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCitric AcidHCID 311—
ReactantBoron TrichlorideHCID 25135—
ReactantButyl chloroformateHCID 61140—
Reactant2-(Pyrrolidin-1-yl)pyridineHCID 11019020—
ReactantHCID 67133186HCID 67133186—
SolventDichloromethaneHCID 6344—
ProductHCID 67133104HCID 6713310469%

Reaction Steps

To a solution of 3-(3-pyrazol-1-ylmethylphenyl)-5-iso-butyl-N-tert-butylthiophene-2-sulfonamide (82.4 mg, 0.191 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 (42.7 mg, 0.288 mmol) and butyl chloroformate (192.6 μL, 1.91 mmol) and the reaction mixture was stirred overnight. Citric acid (5 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 was purified by LCMS (30-100% CH3CN in water) to give the title compound in 69% yield, over two steps, (62.7 mg, 0.132 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08080571B2
Source datasetuspto-grants-2011_12
ORD IDord-ad6af54bcfe84af4918b0c3dab0ab493
Source noteuspto-grants-2011_12