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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 659683Generated: October 30, 2026

Citric Acid → HCID 67132972, compound

https://huagongshe.com/reaction/659683

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCitric AcidHCID 311—
ReactantBoron TrichlorideHCID 25135—
ReactantButyl chloroformateHCID 61140—
Reactant2-(Pyrrolidin-1-yl)pyridineHCID 11019020—
ReactantHCID 67132862HCID 67132862—
SolventDichloromethaneHCID 6344—
ProductHCID 67132972HCID 6713297270%

Reaction Steps

To a solution of 3-(3-imidazo[4,5-b]pyridin-3-ylmethylphenyl)-5-iso-butyl-N-tert-butylthiophene-2-sulfonamide (53.6 mg, 0.111 mmol; see Example 8(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 (32.9 mg, 0.222 mmol) and butyl chloroformate (141.3 μL, 1.11 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 (20-100% CH3CN in water) to give the title compound in 70% yield, over two steps, (41 mg, 0.078 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08080571B2
Source datasetuspto-grants-2011_12
ORD IDord-b7940f79ea144a8382c06969526072e1
Source noteuspto-grants-2011_12