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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1904271Generated: October 25, 2026

Ethyl 7-chloro-1H-pyrazolo[4,3-B]pyridine-6-carboxylate → ethyl 7-n-butylamino-1H-pyrazolo [4,3-b]pyridine-6-carboxylate

https://huagongshe.com/reaction/1904271

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 7-chloro-1H-pyrazolo[4,3-B]pyridine-6-carboxylateHCID 20038759—
SolventButylamineHCID 8007—
Productethyl 7-n-butylamino-1H-pyrazolo [4,3-b]pyridine-6-carboxylateHCID 20038776135.3%

Reaction Steps

Ethyl 7-chloro-1H-pyrazolo[4,3-b]pyridine-6-carboxylate (3.5 g, 15.5 mmol) was dissolved in n-butylamine (25 ml) and stirred at room temperature for 3 h. Excess butylamine was removed in vacuo and the residual solid was washed well with water, and recrystallised from ethyl acetate to give ethyl 7-n-butylamino-1H-pyrazolo [4,3-b]pyridine-6-carboxylate (2.75 g, 67%), m.p. 164°-170° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04837238
Source datasetuspto-grants-1989_06
ORD IDord-c7eda3542d964d179234801c23ff0d71
Source noteuspto-grants-1989_06