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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 643722Generated: October 30, 2026

Pyridine → HCID 57708180, compound

https://huagongshe.com/reaction/643722

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 68615607HCID 68615607—
SolventDichloromethaneHCID 6344—
ProductHCID 57708180HCID 5770818078.6%

Reaction Steps

To a solution of 1-{[1-(cyclopropylmethyl)-2-(2,2-dimethylpropyl)-1H-benzimidazol-5-yl]sulfonyl}-2-methylpropan-2-amine (step G, of EXAMPLE 18, 39 mg, 0.1 mmol) in dichloromethane (0.5 mL) were added pyridine (0.016 mL, 0.2 mmol) and acetic anhydride (0.012 mL, 0.12 mmol) at room temperature. After 4 h, the reaction was quenched by addition of water (10 mL) and the organic layer was separated. The aqueous layer was extracted with dichloromethane (10 mL×2) and the combined organic layer was washed with water (10 mL), brine (5 mL) and dried over sodium sulfate, filtered and concentrated. The residue was purified by silica gel TLC eluting with hexane/ethyl acetate (1/5) to afford 33 mg (78%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07700618B2
Source datasetuspto-grants-2010_04
ORD IDord-c69d584058f44abdab44b259e71bcf1a
Source noteuspto-grants-2010_04