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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 659685Generated: October 30, 2026

Anisole → HCID 67133040, compound

https://huagongshe.com/reaction/659685

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnisoleHCID 7519—
ReactantSodium CarbonateHCID 10340—
ReactantButyl chloroformateHCID 61140—
ReactantHCID 67133227HCID 67133227—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventTrifluoroacetic acidHCID 6422—
ProductHCID 67133040HCID 6713304034%

Reaction Steps

To a solution of 3-[3-(2-acetylimidazol-1-ylmethyl)phenyl]-5-iso-butyl-N-tert-butylthiophene-2-sulfonamide (62.4 mg, 0.132 mmol; see step (b)) in TFA (2 mL) was added anisole (150 μL) and the reaction mixture was stirred overnight at ambient temperature. The reaction mixture was concentrated in vacuo and dried in vacuo overnight. To the crude product dissolved in CH2Cl2 (2 mL) was added Na2CO3 (302 mg, 2.85 mmol), water (0.8 mL) and butyl chloroformate (83.8 μL, 0.659 mmol) and the reaction mixture was stirred overnight at ambient temperature. The reaction mixture was diluted with CH2Cl2 (30 mL) and washed with citric acid (10% aq), brine and water, dried (over anhydrous MgSO4), concentrated in vacuo, and the residue purified by flash chromatography using MeOH:CH2Cl2 (5:95) as eluent to give the title compound as a white solid in 34% yield, over two steps, (23 mg, 0.0045 nmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08080571B2
Source datasetuspto-grants-2011_12
ORD IDord-c84e9b2660594fb7ae7a80dbba54c40e
Source noteuspto-grants-2011_12