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HRID 886942Erstellt: 26. Oktober 2026

Water → tert-butyl 9-(2,4-dimethyl-1,3-thiazol-5-yl)-2,3-dihydro-1,4-benzoxazepine-4(5H)-carboxylate

https://huagongshe.com/reaction/886942

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktSodium CarbonateHCID 10340—
Edukt2,4-Dimethyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,3-thiazoleHCID 18525700—
EduktTert-butyl 9-bromo-2,3-dihydrobenzo[F][1,4]oxazepine-4(5H)-carboxylateHCID 59403519—
KatalysatorHCID 178418397HCID 178418397—
Lösungsmittel1,2-DimethoxyethaneHCID 8071—
Produkttert-butyl 9-(2,4-dimethyl-1,3-thiazol-5-yl)-2,3-dihydro-1,4-benzoxazepine-4(5H)-carboxylateHCID 6857803566,7%

Reaktionsbedingungen

Temperatur85 °C

Reaktionsschritte

A mixture of tert-butyl 9-bromo-2,3-dihydro-1,4-benzoxazepine-4(5H)-carboxylate (328 mg, 1.00 mmol), 2,4-dimethyl-1,3-thiazol-5-ylboronic acid pinacol ester (239 mg, 1.00 mmol), saturated aqueous sodium carbonate solution (6 ml) and tetrakis(triphenylphosphine)palladium(0) (32.6 mg, 0.0282 mmol) in dimethoxyethane (10 ml) was stirred at 85° C. for 12 hr under a nitrogen atmosphere. The reaction mixture was poured into water, and the mixture was extracted with ethyl acetate. The extract was washed with water, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (hexane:ethyl acetate=1:1) to give the desired product (240 mg, 66.7%) as an oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08247403B2
Quelldatensatzuspto-grants-2012_08
ORD IDord-8b1902f754524033aaf3f879b8a9d439
Quellennotizuspto-grants-2012_08