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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1534406Generated: November 4, 2026

Propargyl bromide → methyl 5-[N-tert-butoxycarbonyl-N-(prop-2-ynyl)amino]pyridine-2-carboxylate

https://huagongshe.com/reaction/1534406

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropargyl bromideHCID 7842—
ReactantMethyl 5-(tert-Butoxycarbonylamino)picolinateHCID 14842342—
Productmethyl 5-[N-tert-butoxycarbonyl-N-(prop-2-ynyl)amino]pyridine-2-carboxylateHCID 1484234390%

Reaction Steps

Using the method described in J. Med. Chem., 1980, 23, 1405, methyl 5-(N-tert-butoxycarbonylamino)pyridine-2-carboxylate was reacted with prop-2-ynyl bromide to give methyl 5-[N-tert-butoxycarbonyl-N-(prop-2-ynyl)amino]pyridine-2-carboxylate in 90% yield. A mixture of the product so obtained and trifluoroacetic acid was stirred at 0° C. for 1 hour and evaporated. There was thus obtained methyl 5-(N-prop-2-ynylamino)pyridine-2-carboxylate in 90% yield, as a gum.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05089499
Source datasetuspto-grants-1992_02
ORD IDord-80acd854d3f0420a9e16cd6c2acfb20b
Source noteuspto-grants-1992_02