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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2404458Generated: October 31, 2026

Acetic Anhydride → Ammonia methanol dichloromethane

https://huagongshe.com/reaction/2404458

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 178480514HCID 178480514—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventAcetonitrileHCID 6342—
ProductAmmonia methanol dichloromethaneHCID 21584172—
ProductHCID 178475105HCID 178475105—

Reaction Steps

To a solution of N-(2-{3-[(1H-benzimidazol-2-yl)(1-methylpiperidin-4-yloxy)-methyl]phenylsulfanyl}ethyl)guanidine.dihydrochloride (100 mg) in dry acetonitrile (1 mL) is added acetic anhydride (64 mg) et 4-dimethylaminopyridine (51 mg). After 24 hours at room temperature, solvent and volatiles are removed under reduced pressure. The residue is purified by chromatography (toluene/acetone/triethylamine 50/50/1 then gradient dichloromethane/methanol/ammonia from 95/5/0.5 to 90/10/1) to give N-acetyl-N′-(2-{3-[(1H-benzimidazol-2-yl)(1-methylpiperidin-4-yloxy)methyl]phenylsulfanyl}ethyl)guanidine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08802664B2
Source datasetuspto-grants-2014_08
ORD IDord-c3ab9301ce3a4451b51814c208a8678b
Source noteuspto-grants-2014_08