Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium formate | HCID 2723923 | — |
| Reactant | HCID 86677112 | HCID 86677112 | — |
| Solvent | Formic Acid | HCID 284 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 67107513 | HCID 67107513 | 27.8% |
Reaction Steps
A mixture of methyl 6-(benzenesulphonylmethyl)-3-(2-bromoacetyl)-2-methoxy-benzoate (Intermediate 51, 0.9 g) and ammonium formate (0.45 g) in formic acid (5 ml) was sealed in a vial and heated at 80° C. for 3 hours then at 100° C. for 6 hours. After standing at room temperature overnight, the mixture was heated at 120° C. for 4 hours. The mixture was diluted with water and extracted with ethyl acetate, dried (MgSO4) and filtered. The filtrate was evaporated to dryness to give methyl 6-(benzenesulphonylmethyl)-3-(oxazol-4-yl)-2-methoxy-benzoate (0.22 g) as a yellow gum which was used directly without further purification or characterisation.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09067905B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-115b976239ba4e1a8fb606f6d0c1ef2d |
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| Source note | uspto-grants-2015_06 |
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