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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 326822Generated: October 25, 2026

Acetic Anhydride → Lcb-2183

https://huagongshe.com/reaction/326822

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantAminopyrazine carboxamideHCID 280292—
ProductLcb-2183HCID 135418284—

Reaction Steps

A mixture of 8.3 g (0.060 mole) of 3-amino-2-pyrazinecarboxamide [prepared according to R. C. Ellingson et al., J. Am. Chem. Soc. 1945, 67, 1711], 49.5 g (0.24 mole) of triethyl orthoethoxyacetate [prepared according to S. M. McElvain and P. M. Walters, J. Am. Chem. Soc. 1942, 64, 1963] and 53 ml of acetic anhydride is refluxed under a nitrogen atmosphere for 3 hours. The temperature of this reflux falls with the passage of time from 124° to 96° C. and then remains constant at the latter temperature. After cooling, the precipitate formed is isolated by filtration. It is washed with ether and recrystallized from ethanol. Yld: 5.5 g (44%), m.p. 168°-169° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05270465
Source datasetuspto-grants-1993_12
ORD IDord-bcc0a662e5b9459f8591ede3b1f25430
Source noteuspto-grants-1993_12