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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2304775Generated: October 26, 2026

Methanol → Famciclovir

https://huagongshe.com/reaction/2304775

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantAcetic AnhydrideHCID 7918—
ReactantTriethylamineHCID 8471—
ReactantDesacetyl famciclovir hydrochlorideHCID 44226540—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventIsopropanolHCID 3776—
SolventDichloromethaneHCID 6344—
ProductFamciclovirHCID 332470%

Reaction Steps

To a stirred suspension of 2-amino-9-(4-hydroxy-3-hydroxymethylbut-1-yl)purine hydrochloride (0.79 g), 4-dimethylaminopyridine (16 mg) and triethylamine (1.4 ml) in dichloromethane (16 ml) at room temperature was added acetic anhydride (0.57 ml). The resulting mixture was stirred at ambient temperature for 2.25 hours. Methanol (4 ml) was added and the solution stirred for 30 min before being evaporated to dryness. Water (20 ml) was added and the aqueous solution extracted with dichloromethane (3×20 ml). The combined extracts were concentrated to give an oil. This oil was dissolved in 2-propanol (5 ml), the solvent evaporated and the residue recrystallised from 2-propanol (5 ml). The product was collected by filtration, washed with 2-propanol (3 ml) and dried to give the title compound (654 mg, 70%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06437125B1
Source datasetuspto-grants-2002_08
ORD IDord-35dc21db3cee496a865be298f70546e9
Source noteuspto-grants-2002_08