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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1269892생성일: 2026년 10월 25일

18-Crown-6 → tert-butyl 4-{1-(2-tetrahydropyranyl)-1H-indazol-5-ylamino}benzoate

https://huagongshe.com/reaction/1269892

반응식

참여 물질

역할이름HCID투입량
반응물18-Crown-6HCID 28557—
반응물Methyl 4-acetamido-2,5-dimethylbenzoateHCID 327521—
반응물Binap, (A+-)-HCID 634876—
반응물Tert-butyl 4-bromobenzoateHCID 11334366—
반응물1-(Oxan-2-yl)-1H-indazol-5-amineHCID 22933927—
반응물Sodium t-butoxideHCID 23676156—
용매TolueneHCID 1140—
용매Diethyl EtherHCID 3283—
생성물tert-butyl 4-{1-(2-tetrahydropyranyl)-1H-indazol-5-ylamino}benzoateHCID 6943310456%

반응 단계

In a two-necked flask the inner atmosphere of which had been replaced with nitrogen were placed tert-butyl 4-bromobenzoate (2.57 mg, 1.00 mmol), toluene (2 ml), 18-crown-6 (380 mg, 1.40 mmol), the 1-(2-tetrahydropyranyl)-1H-indazol-5-amine (261 mg, 1.23 mmol) obtained in Example 317, (e) and sodium tert-butoxide (135 mg, 1.40 mmol) in that order. After the inner atmosphere of the flask was replaced with nitrogen again, tris(dibenzylideneacetone)(chloroform) dipalladium(0) (52 mg, 0.050 mmol) and (S)-2,2′-bis(diphenylphophino)-1,1′-binaphthyl (94 mg, 0.151 mmol) were added. After the third replacement of the inner atmosphere of the flask with nitrogen, stirring was conducted at 80° C. for 8 hours. The resulting mixture was diluted with diethyl ether and the solid was removed by filtration using Celite. Then, the solvent was distilled off under reduced pressure to obtain a crude product. The crude product was purified by a silica gel column chromatography (eluent: hexane/ethyl acetate=3/1) to obtain tert-butyl 4-{1-(2-tetrahydropyranyl)-1H-indazol-5-ylamino}benzoate (218 mg, 56%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07199147B2
출처 데이터셋uspto-grants-2007_04
ORD IDord-7171331d452549a1932e5a6d8ccbf5ae
출처 메모uspto-grants-2007_04