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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1093944Generated: November 1, 2026

Pyridine → HCID 59623721, compound

https://huagongshe.com/reaction/1093944

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantMethyl 3-aminopyrazinecarboxylateHCID 72669—
ReactantHCID 59623758HCID 59623758—
SolventDichloromethaneHCID 6344—
ProductHCID 59623721HCID 59623721—

Reaction Steps

To a solution of 3-amino-pyrazine-2-carboxylic acid methyl ester (commercially available) (2.0 g) and (2-chloro-5-trifluoromethyl-phenyl)-methanesulfonyl chloride (Example 1.2) (4.2 g) in dichloromethane (32 ml) was added dropwise pyridine (5.3 ml) over a period of 5 minutes at ambient temperature. The reaction mixture was stirred at ambient temperature for 23 hours. Dichloromethane (50 ml) was added to the reaction mixture and the mixture was washed with aqueous sulfuric acid (2M) (3×30 ml). The phases were separated and the organic layer was concentrated. The residue was purified by column chromatography on silica gel (eluent: ethyl acetate/dichloromethane from 0:10 to 1:9) to give 3-(2-chloro-5-trifluoromethyl-phenylmethanesulfonylamino)-pyrazine-2-carboxylic acid methyl ester as a white solid (4.728 g). 1H-NMR (400 MHz, CDCl3): 10.30 (s, 1H), 8.59 (s, 1H), 8.47 (s, 1H), 7.77 (bs, 1H), 7.54-7.60 (m, 2H), 5.15 (s, 2H), 4.04 (s, 3H) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08133849B2
Source datasetuspto-grants-2012_03
ORD IDord-9108254a01f44c6d80a2e1ac3cf5d0e2
Source noteuspto-grants-2012_03