Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1166706Generated: October 25, 2026

Dimethylformamide → (R)-9-[2(L-Valyloxymethyl)-4-(stearoyloxy)butyl]guanine

https://huagongshe.com/reaction/1166706

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantBoc-L-ValineHCID 83693—
Reactant(R)-9-[2-Hydroxymethyl-4-(stearoyloxy)butyl]guanineHCID 136343267—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Product(R)-9-[2(L-Valyloxymethyl)-4-(stearoyloxy)butyl]guanineHCID 13542339545.7%

Reaction Steps

A mixture of N-Boc-L-valine (528 mg; 2.1 mmol) and N,N′-dicyclohexyl carbodiimide (250 mg; 1.21 mmol) in dichloromethane (20 ml) was stirred over night at room temperature, dicyclohexylurea filtered off and extracted with a small volume of dichloromethane, and the filtrate evaporated in vacuo to a small volume. (R)-9-[2-Hydroxymethyl-4-(stearoyloxy)butyl]guanine (340 mg; 0.654 mmol), 4-dimethylaminopyridine (25 mg; 0.205 mmol), and dry N,N-dimethylformamide (15 ml) were added and the mixture was stirred for 4 h at 50° C. under N2. The solvent was evaporated in vacuo to a small volume. Column chromatography on silica gel, then on aluminum oxide (ethyl acetate:methanol: water 15:2:1 as eluent) gave 185 mg (39%) pure title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06613936B1
Source datasetuspto-grants-2003_09
ORD IDord-ce81f07cfd82409393aacfb14c15ee65
Source noteuspto-grants-2003_09