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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1268155Generated: October 25, 2026

Methanol → Famciclovir

https://huagongshe.com/reaction/1268155

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 0.5 hours 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 numberUS06555685B1
Source datasetuspto-grants-2003_04
ORD IDord-dfd0fd26c1a749f19a918feecabcbf28
Source noteuspto-grants-2003_04