Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | HCID 66882748 | HCID 66882748 | — |
| Catalyst | Thionyl Chloride | HCID 24386 | — |
| Product | HCID 66881176 | HCID 66881176 | — |
Reaction Steps
A stirred suspension of (1RS,2SR)-2-[2-fluoro-4-(2-oxo-2H-pyridin-1-yl)-phenylcarbamoyl]-cyclopropanecarboxylic acid (140 mg) in MeOH (5 ml) was cooled to 0° C. and treated with thionyl chloride (10 drops). The mixture turned immediately into a clear solution. Stirring was continued for 3 hrs at 0° C. Then the reaction mixture was concentrated. The crude product was purified by column chromatography (silica gel; gradient: CH2Cl2−>CH2Cl2/MeOH) to give (1RS,2SR)-2-[2-fluoro-4-(2-oxo-2H-pyridin-1-yl)-phenylcarbamoyl]-cyclopropanecarboxylic acid methyl ester (84 mg) as colorless amorphous solid. MS: 353.4 ([M+H]+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07501413B2 |
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| Source dataset | uspto-grants-2009_03 |
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| ORD ID | ord-d491ba9104c64357b1bf083aa7de18f9 |
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| Source note | uspto-grants-2009_03 |
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