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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 982877Generated: October 30, 2026

Methanol → HCID 178456427, compound

https://huagongshe.com/reaction/982877

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantAmmonium formateHCID 2723923—
ReactantHCID 178456428HCID 178456428—
CatalystPalladiumHCID 23938—
SolventWaterHCID 962—
ProductHCID 178456427HCID 178456427169.3%

Reaction Steps

Add to a solution of trans-{4-[6-(1-benzyl-piperidin-4-ylamino)-9-isopropyl-9H-purin-2-ylamino]-cyclohexyl}-carbamic acid tert-butyl ester (8b, 1 g, 1 mmol) and methanol (40 ml), a suspension of palladium black (0.25 g) in a little water. Then add a solution of ammonium formate (0.4 mg, 6.4 mmol) and 10 ml of water, and reflux overnight. Filter the reaction through Celite® and concentrate the filtrate to dryness. Dissolve the residue in methylene chloride (50 ml), extracted with water, and filter through Celite® to remove a milky white precipitate. Separate the organic layer, wash with brine, dry over sodium sulfate, filter and concentrate the filtrate to dryness. Purify the residue on a 40 gram silica gel column (Biotage) using DCM/methanol (4:1) to give 0.8 grams of trans-{4-[9-isopropyl-6-(piperidin-4-ylamino)-9H-purin-2-ylamino]-cyclohexyl}-carbamic acid tert-butyl ester (9b).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06861524B2
Source datasetuspto-grants-2005_03
ORD IDord-d455eb2354ff4477979a3c31b73e2c12
Source noteuspto-grants-2005_03