Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | HCID 178507937 | HCID 178507937 | — |
| Product | HCID 178475837 | HCID 178475837 | — |
| Product | HCID 178522442 | HCID 178522442 | — |
Reaction Steps
4-(2,6-Difluoro-benzoylamino)-1H-pyrazole-3-carboxylic acid (2-amino-3-hydroxymethyl-phenyl)-amide (100 mg, 0.26 mmol) was dissolved in acetic acid (10 ml) then heated for 10 min at 150° C. (100 W) in a CEM discover microwave synthesiser. The reaction mixture was reduced then azeotroped with toluene (2×20 ml). The residue was purified by flash column chromatography [SiO2, EtOAc-hexane (1:1, 2:1, 3:1)] to give 2,6-difluoro-N-[3-(4-hydroxymethyl-1H-benzimidazol-2-yl)-1H-pyrazol-4-yl]-benzamide (25 mg) as an off white solid (LC/MS: Rt 2.70, [M+H]+ 370) and acetic acid 2-[4-(2,6-difluoro-benzoylamino)-1H-pyrazol-3-yl]-1H-benzimidazol-4-ylmethyl ester (20 mg) as an off white solid. (LC/MS: Rt 3.60, [M+H]+ 412).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07977477B2 |
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| Source dataset | uspto-grants-2011_07 |
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| ORD ID | ord-cf3c45538fd14d579f36ccaa249d1b22 |
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| Source note | uspto-grants-2011_07 |
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