Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 580483Generated: November 1, 2026

2-Pyrazinecarboxylic acid → HCID 13983402, compound

https://huagongshe.com/reaction/580483

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Pyrazinecarboxylic acidHCID 1047—
Reactant7-Chloro-1,8-naphthyridin-2-amineHCID 85199—
ProductHCID 13983402HCID 1398340268.4%

Reaction Conditions

Temperature25 °C

Reaction Steps

The procedure is similar to that described in Example 1, but starting with 2-pyrazinecarboxylic acid (7.5 g), N,N'-carbonyldiimidazole (9.7 g) and 2-amino-7-chloro-1,8-naphthyridine (10.8 g). The insoluble product is separated by filtration, washed with tetrahydrofuran (3×50 cc) and then with water (300 cc) and dried in the air. The product is suspended in acetonitrile (100 cc), stirred for 1 hour at 25° C. and separated by filtration, and then dried at 50° C. under reduced pressure (0.07 kPa). N-(7-Chloro-1,8-naphthyridin-2-yl)-2-pyrazinecarboxamide (11.75 g), m.p. 308° C., is thereby obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04753941
Source datasetuspto-grants-1988_06
ORD IDord-bc4b47d6dc4244d08cd26b201ee530c5
Source noteuspto-grants-1988_06