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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1723426Generated: November 4, 2026

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

https://huagongshe.com/reaction/1723426

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 numberUS04861785
Source datasetuspto-grants-1989_08
ORD IDord-0741c64fcd4d4a8182e8eaa4281e7181
Source noteuspto-grants-1989_08