돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 473856생성일: 2026년 10월 25일

Potassium Carbonate → tert-butyl 7-(thiazol-5-yl)-2,3-dihydrobenzo[f][1,4]oxazepine-4(5H)-carboxylate

https://huagongshe.com/reaction/473856

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물5-BromothiazoleHCID 546059—
반응물Tert-butyl 7-(tetramethyl-1,3,2-dioxaborolan-2-yl)-2,3,4,5-tetrahydro-1,4-benzoxazepine-4-carboxylateHCID 66820441—
촉매Palladium ChlorideHCID 24290—
촉매Ferrocene-1,1'-bis-(diphenylphosphine)HCID 635956—
용매Ethyl AcetateHCID 8857—
용매N,N-Dimethylacetamide--water (1/1)HCID 21534740—
생성물tert-butyl 7-(thiazol-5-yl)-2,3-dihydrobenzo[f][1,4]oxazepine-4(5H)-carboxylateHCID 6751397570%

반응 단계

A solution of tert-butyl 7-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2,3-dihydrobenzo[f][1,4]oxazepine-4(5H)-carboxylate (73 mg, 0.19 mol), 5-bromothiazole (40 mg, 0.26 mmol), 1,1′-Bis(diphenylphosphino)ferrocene]dichloropalladium(II) (22 mg, 0.03 mmol) and potassium carbonate (0.14 g, 1.0 mmol) in N,N-dimethylacetamide/water 5:1 (5.5 mL) was heated to 90° C. for 1 hour. The cooled reaction mixture was diluted with ethyl acetate (50 mL) and washed with water (30 mL) and brine (20 mL), and then dried over anhydrous sodium sulfate and concentrated. Purified by silica gel column chromatography (ethyl acetate/hexanes, 1:2) to give tert-butyl 7-(thiazol-5-yl)-2,3-dihydrobenzo[f][1,4]oxazepine-4(5H)-carboxylate (44 mg, 70% yield). MS (EI) for C17H20N2O3S: 333 (MH+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08637499B2
출처 데이터셋uspto-grants-2014_01
ORD IDord-663fc8696a014b818c16a72c00f6be7c
출처 메모uspto-grants-2014_01