Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,6-Lutidine | HCID 7937 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | HCID 18180195 | HCID 18180195 | — |
| Reactant | 1-[2-[(Trimethylsilyl)methoxy]ethyl]-1H-pyrazole-5-carboxylic acid | HCID 67398926 | — |
| Catalyst | Dimethylformamide | HCID 6228 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 57799150 | HCID 57799150 | — |
Reaction Steps
Oxalyl chloride (0.17 ml, 1.9 mmol) was added to a slurry of 2-(2-trimethylsilanylmethoxy-ethyl)-2H-pyrazole-3-carboxylic acid) (Heterocycles (1992) 34 303-314), (428 mg, 1.76 mmol) in dichloromethane (15 ml), 1 drop of dimethylformamide was added and the reaction stirred at room temperature under N2 for 1 hour before concentrating in vacuo and azeotroping with dichloromethane. The resulting acid chloride was dissolved in 5 ml acetonitrile and added to a solution of 3-(2,5-dichloro-phenyl)pyrazine-2,6-diamine (Preparation 11, 300 mg, 1.18 mmol) in acetonitrile (15 ml) and 2,6-lutidine (0.21 ml, 1.8 mmol). The reaction was stirred at room temperature under N2 for 72 hours before concentrating in vacuo then partitioning between 50 ml ethyl acetate and 50 ml water. The organic layer was dried over MgSO4 and concentrated in vacuo to give a brown oil which was purified by column chromatography (ethyl acetate, heptane, 1:2) to give 52 mg of the title product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07572797B2 |
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| Source dataset | uspto-grants-2009_08 |
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| ORD ID | ord-33a657c2ac13400dadb592821632972f |
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| Source note | uspto-grants-2009_08 |
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