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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1930185Generated: October 25, 2026

Ammonia → 6-(4'-(2-Amino-2-oxoethyl)-2'-chlorobiphenyl-4-yl)-3,5-dimethylpyrazine-2-carboxamide

https://huagongshe.com/reaction/1930185

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantMethyl 2-(4'-(6-carbamoyl-3,5-dimethylpyrazin-2-yl)-2-chlorobiphenyl-4-yl)acetateHCID 59627714—
Product6-(4'-(2-Amino-2-oxoethyl)-2'-chlorobiphenyl-4-yl)-3,5-dimethylpyrazine-2-carboxamideHCID 4984724428%

Reaction Conditions

Temperature140 °C

Reaction Steps

Methyl 2-(4′-(6-carbamoyl-3,5-dimethylpyrazin-2-yl)-2-chlorobiphenyl-4-yl)acetate (Intermediate 1-1; 60 mg, 0.15 mmol) and ammonia (7M in methanol) (2091 μL, 14.64 mmol) were sealed into a microwave tube. The reaction was heated to 140° C. for 1 hour in the microwave reactor and cooled to RT. Removal of the solvent under reduced pressure gave crude product. The crude product was purified by preparative HPLC (Waters—Xbridge Prep C18 5 μm), using decreasingly polar mixtures of water (containing 0.1% formic acid) and {MeOH(3):MeCN(1)} as eluents. Fractions containing the desired compound were evaporated to dryness to afford 6-(4′-(2-amino-2-oxoethyl)-2′-chlorobiphenyl-4-yl)-3,5-dimethylpyrazine-2-carboxamide (16.20 mg, 28.0%) as a colourless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08188092B2
Source datasetuspto-grants-2012_05
ORD IDord-a8fb1d4eec8b422cb98909dc22b42180
Source noteuspto-grants-2012_05