Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 2-Methoxybenzoyl chloride | HCID 88969 | — |
| Reactant | HCID 86588739 | HCID 86588739 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 22276525 | HCID 22276525 | — |
Reaction Steps
To a mixture of N-(2-tetrahydropyranyloxy-2-[7-(5-(4-chlorophenyl)-2-thienyl)-1,1-dioxoperhydro-1,4-thiazepin-7-yl]acetamide (90 mg) and pyridine (0.5 ml) in chloroform (3 ml) was added 2-methoxybenzoyl chloride (37 mg) and the mixture was stirred at ambient temperature for 3 hours. The mixture was pertitioned between water and chloroform. The organic layer was separated, washed with 5% citric acid water solution, water, saturated sodium bicarbonate solution and brine. To the reaction mixture were added 4N hydrogen chloride-ethyl acetate solution (0.5 ml), chloroform (1 ml) and methanol (1.5 ml) and the reaction mixture was stirred at ambient temperature for 30 minutes. After evaporation of solvent, the residue was purified by HPLC (0.1% trifluoroacetic acid in 20% acetonitrile-water ˜0.1% trifluoroacetic acid in 80% acetonitrile-water) to give N-hydroxy-2-[7-(5-(4-chlorophenyl)-2-thienyl)-4-(2-methoxybenzoyl)-1,1-dioxoperhydro-1,4-thiazepin-7-yl]acetamide (54 mg) as a pale yellow powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06967197B2 |
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| Source dataset | uspto-grants-2005_11 |
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| ORD ID | ord-0d2daa5a34b04373b35a912865d27c31 |
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| Source note | uspto-grants-2005_11 |
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