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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2248803Generated: October 30, 2026

Ammonia → HCID 19785352, compound

https://huagongshe.com/reaction/2248803

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantHCID 19785231HCID 19785231—
CatalystMercuric oxideHCID 30856—
SolventMethanolHCID 887—
ProductHCID 19785352HCID 1978535292.1%

Reaction Steps

A mixture of 24 parts of ethyl 4-[[[[4-[(phenylmethyl)amino]-5-pyrimidinyl]amino]thioxomethyl]amino]-1-piperidinecarboxylate, 24 parts of mercury(II) oxide and 240 parts of methanol, saturated with ammonia was stirred overnight at reflux temperature. The reaction mixture was filtered while hot and the filtrate was evaporated. The residue was taken up in a mixture of trichloromethane and ethanol. After washing with water, the organic layer was evaporated and the residue was crystallized from acetonitrile. The product was filtered off and dried, yielding 20.3 parts (92.1%) of ethyl 4-[[9-(phenylmethyl)-9H-purin-8-yl]amino]-1-piperidinecarboxylate; mp. 156.9° C. (compound 9).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05041448
Source datasetuspto-grants-1991_08
ORD IDord-97cc647595e5402985b2704b4fb500fc
Source noteuspto-grants-1991_08