Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 659680Generated: October 30, 2026

Citric Acid → HCID 67133142, compound

https://huagongshe.com/reaction/659680

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCitric AcidHCID 311—
ReactantBoron TrichlorideHCID 25135—
ReactantButyl chloroformateHCID 61140—
Reactant2-(Pyrrolidin-1-yl)pyridineHCID 11019020—
ReactantHCID 67133102HCID 67133102—
SolventDichloromethaneHCID 6344—
ProductHCID 67133142HCID 6713314273%

Reaction Steps

To a solution of 3-[3-(2-ethylimidazol-1-ylmethyl)phenyl]-5-iso-butyl-N-tert-butylthiophene-2-sulfonamide (55.1 mg, 0.120 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, concentrated in vacuo. To the crude product dissolved in pyridine (1.5 mL) was added pyrrolidinopyridine (35.5 mg, 0.240 mmol) and butyl chloroformate (152.5 μL, 1.20 mmol) and the reaction mixture was stirred overnight. Citric acid (3 mL, 10% aq) was added to the reaction mixture, extracted with EtOAc, dried (over anhydrous MgSO4), concentrated in vacuo, and the residue was purified by flash chromatography using MeOH:CH2Cl2 (5:95 to 8:92) as eluent to give the title compound in 73% yield, over two steps, (44.3 mg, 0.088 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08080571B2
Source datasetuspto-grants-2011_12
ORD IDord-e06a0e86177541f2b5464cb2de5ccf6d
Source noteuspto-grants-2011_12