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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 362610Generated: October 25, 2026

Ammonium formate → HCID 54149671, compound

https://huagongshe.com/reaction/362610

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium formateHCID 2723923—
Reactant(R)-2-Amino-9-(2-stearoyloxymethyl-4-(N-tert-butoxycarbonyl-L-valyloxy)butyl)-6-chloropurineHCID 53751265—
CatalystPalladiumHCID 23938—
SolventEthylacetate methanolHCID 21584119—
ProductHCID 54149671HCID 54149671—

Reaction Steps

To the solution of (R)-2-amino-9-(2-stearoyloxymethyl-4-(N-tert-butoxycarbonyl-L-valyloxy)butyl)-6-chloropurine (240 mg, 0.33 mmole) in methanol/ethyl acetate (6 ml, 3:1 V/V) were added ammonium formate (105 mg, 1.65 mmole) and 10% palladium on carbon (15 mg). The reaction was kept under reflux for 1 hour and recharged with ammonium formate (70 mg). After one hour more the TLC showed completion of the reaction and the mixture was filtered through Celite and washed extensively with ethanol. The filtrate was evaporated and purified by silica gel column. Yield: 193 mg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05869493
Source datasetuspto-grants-1999_02
ORD IDord-a2eb9cc776ff4d149f2d1f0003c49716
Source noteuspto-grants-1999_02