HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1063918Generated: November 1, 2026
{3-[(Methylcarbamoyl)amino]phenyl}boronic acid → HCID 86588734, compound
https://huagongshe.com/reaction/1063918
Participants
| Role | Name | HCID | Charge |
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| Reactant | {3-[(Methylcarbamoyl)amino]phenyl}boronic acid | HCID 22276448 | — |
| Reactant | HCID 23402085 | HCID 23402085 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Sodium Carbonate | HCID 10340 | — |
| Product | HCID 86588734 | HCID 86588734 | 13.4% |
Reaction Steps
A mixture of N-(2-tetrahydropyranyloxy)-2-[(S)-7-(5-bromo-2-thienyl)-4-methanesulfonyl-1,1-dioxoperhydro-1,4-thiazepin-7-yl]acetamide (230 mg), 3-(methylaminocarbonylamino)phenylboronic acid (123 mg) and tetrakis(triphenylphosphine)palladium(0) (24.4 mg) in a mixture of 1,2-dimethoxyethane (2 ml) and 2M aqueous sodium carbonate solution (0.85 ml) was stirred for 4 hours at 80° C. After cooling to room temperature, the mixture was diluted with ethyl acetate, washed with aqueous saturated sodium bicarbonate and brine, dried over sodium sulfate and concentrated in vacuo. The obtained residue was dissolved in methanol (2 ml) and 10% hydrogen chloride in methanol (0.5 ml) was added thereto. After being stirred for 30 minutes at room temperature, the solution was concentrated in vacuo. The residue was purified with silica gel column chromatography (eluent; 0.5-5% methanol in chloroform) to give N-hydroxy-2-[(S)-7-(5-(3-(methylaminocarbonylamino)-phenyl)-2-thienyl)-4-methanesulfonyl-1,1-dioxoperhydro-1,4-thiazepin-7-yl]acetamide (30 mg).
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-778b49d90fa146b7bd43de5cfeab5e66 |
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| Source note | uspto-grants-2005_11 |
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