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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2173720Generated: November 1, 2026

Triethylamine → HCID 178499186, compound

https://huagongshe.com/reaction/2173720

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPyBOPHCID 2724699—
ReactantIsohexane ethyl acetateHCID 21882781—
Reactant3-Amino-6-bromo-5-trifluoromethyl-pyrazine-2-carboxylic acidHCID 58442296—
ReactantHCID 178499187HCID 178499187—
SolventDichloromethaneHCID 6344—
SolventAcetonitrile--water (1/1)HCID 18373917—
ProductHCID 178499186HCID 178499186—

Reaction Steps

To a solution of 3-amino-6-bromo-5-trifluoromethyl-pyrazine-2-carboxylic acid (Intermediate 2) (300 mg, 1.049 mmol) in dry DCM (10 ml) was added NEt3 (0.322 ml, 2.308 mmol) followed by methyl 5-amino-1H-1,2,4-triazole-3-carboxylate (149 mg, 1.049 mmol). After stirring at RT for 5 minutes the reaction mixture was treated with PyBOP (546 mg, 1.049 mmol) and stirred for 3 hours. The mixture was partitioned between DCM (20 ml) and water (20 ml), shaken and separated. The organic portion was washed with water (20 ml), dried over MgSO4, filtered and concentrated in vacuo to give an orange oil. Purification of the crude residue by chromatography on silica eluting with 0-100% EtOAc in iso-hexane, followed by 0-35% MeOH in EtOAc afforded a yellow oil. Trituration of the oil with EtOAc/iso-hexane followed by MeCN/water afforded the title compound as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09056867B2
Source datasetuspto-grants-2015_06
ORD IDord-b4eb6f5f58d14092883b444fd63d1ebb
Source noteuspto-grants-2015_06