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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant{3-[(Methylcarbamoyl)amino]phenyl}boronic acidHCID 22276448—
ReactantHCID 23402085HCID 23402085—
CatalystHCID 178418397HCID 178418397—
Solvent1,2-DimethoxyethaneHCID 8071—
SolventEthyl AcetateHCID 8857—
SolventSodium CarbonateHCID 10340—
ProductHCID 86588734HCID 8658873413.4%

Reaction Conditions

Temperature80 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06967197B2
Source datasetuspto-grants-2005_11
ORD IDord-778b49d90fa146b7bd43de5cfeab5e66
Source noteuspto-grants-2005_11