Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | PyBOP | HCID 2724699 | — |
| Reactant | Isohexane ethyl acetate | HCID 21882781 | — |
| Reactant | 3-Amino-6-bromo-5-trifluoromethyl-pyrazine-2-carboxylic acid | HCID 58442296 | — |
| Reactant | HCID 178499187 | HCID 178499187 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Acetonitrile--water (1/1) | HCID 18373917 | — |
| Product | HCID 178499186 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09056867B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-b4eb6f5f58d14092883b444fd63d1ebb |
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| Source note | uspto-grants-2015_06 |
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