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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2248808Generated: October 29, 2026

Isopropanol → 9-(2-furanylmethyl)-N-(4-piperidinyl)-9H-purin-8-amine hemihydrate

https://huagongshe.com/reaction/2248808

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropanolHCID 3776—
ReactantPotassium HydroxideHCID 14797—
Reactantethyl 4-[[9-(2-furanylmethyl)-9H-purin-8-yl]amino]-1-piperidinecarboxylateHCID 19785341—
SolventWaterHCID 962—
Product9-(2-furanylmethyl)-N-(4-piperidinyl)-9H-purin-8-amine hemihydrateHCID 67878730—

Reaction Steps

A mixture of 60.5 parts of ethyl 4-[[9-(2-furanylmethyl)-9H-purin-8-yl]amino]-1-piperidinecarboxylate, 90 parts of potassium hydroxide, 800 parts of 2-propanol and 20 parts of water was stirred for 48 hours at reflux temperature. The reaction mixture was evaporated. The reaction mixture was poured into water while stirring. The product was filtered off and dried, yielding a first fraction of 36.2 parts of 9-(2-furanylmethyl)-N-(4-piperidinyl)-9H-purin-8-amine hemihydrate. The aqueous phase was extracted with dichloromethane. The organic layer was dried, filtered and evaporated. The oily residue was stirred in acetonitrile and 2,2'-oxybispropane. The product was filtered off and dried, yielding a second fraction of 5.6 parts of 9-(2-furanylmethyl)-N-(4-piperidinyl)-9H-purin-8-amine. Total yield 41.8 parts (86%) of 9-(2-furanylmethyl)-N-(4-piperidinyl)-9H-purin-8-amine hemihydrate; mp. 164.1° C. (compound 33).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05041448
Source datasetuspto-grants-1991_08
ORD IDord-8276feb143e44e58b3cb35a5036337de
Source noteuspto-grants-1991_08