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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1085676Generated: November 1, 2026

Ethyl 4-amino-1-piperidinecarboxylate → Ethyl 4-[(thiazolo[4,5-c]pyridin-2-yl)amino]-1-piperidinecarboxylate

https://huagongshe.com/reaction/1085676

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 4-amino-1-piperidinecarboxylateHCID 100867—
Reactant2-(Methylsulfonyl)thiazolo[4,5-c]pyridineHCID 15725138—
SolventChloroformHCID 6212—
ProductEthyl 4-[(thiazolo[4,5-c]pyridin-2-yl)amino]-1-piperidinecarboxylateHCID 1457603176%

Reaction Steps

A mixture of 8.5 parts of ethyl 4-amino-1-piperidinecarboxylate and 2.6 parts of 2-(methylsulfonyl)thiazolo[4,5-c]pyridine was molten together for 1 hour at 120° C. After cooling, the mixture was taken up in trichloromethane. The whole was washed with water and sodium hydroxide, dried, filtered and evaporated. The residue was purified by column chromatography over silica gel using a mixture of trichloromethane and methanol (99:1 by volume) as eluent. The pure fractions were collected and the eluent was evaporated. The residue was stirred in warm 2,2'-oxybispropane. The product was filtered off and dried, yielding 2.8 parts (76%) of ethyl 4-[(thiazolo[4,5-c]-pyridin-2-yl)amino]-1-piperidinecarboxylate; mp. 213° C. (66).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05010198
Source datasetuspto-grants-1991_04
ORD IDord-48576458e8fe4f79ad8f22a658421cc7
Source noteuspto-grants-1991_04