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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2353967생성일: 2026년 10월 26일

3,5-Bis(trifluoromethyl)benzylamine → 5-(3,5-Bis-trifluoromethyl-benzylamino)-8-chloro-2,3,4,5-tetrahydro-benzo[b]azepine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/2353967

반응식

참여 물질

역할이름HCID투입량
반응물3,5-Bis(trifluoromethyl)benzylamineHCID 521099—
반응물Sodium borohydrideHCID 4311764—
반응물tert-Butyl 8-chloro-5-oxo-2,3,4,5-tetrahydro-1H-benzo[b]azepine-1-carboxylateHCID 68678967—
촉매Titanium isopropoxideHCID 11026—
용매MethanolHCID 887—
용매WaterHCID 962—
용매Ethyl AcetateHCID 8857—
생성물5-(3,5-Bis-trifluoromethyl-benzylamino)-8-chloro-2,3,4,5-tetrahydro-benzo[b]azepine-1-carboxylic acid tert-butyl esterHCID 8661608293%

반응 단계

Add 3,5-bis(trifluoromethyl)benzylamine (3.2 g, 13.1 mmol) followed by titanium isopropoxide (5.0 mL) to 8-Chloro-5-oxo-2,3,4,5-tetrahydro-benzo[b]azepine-1-carboxylic acid tert-butyl ester (3.5 g, 11.9 mmol) and stir at room temperature overnight. Dilute the mixture with 20 mL of Methanol and add sodium borohydride (23.8 mmol). Stir the suspension at room temperature for 1 h then dilute with water (200 mL) and ethyl acetate (200 mL). Filter the resulting emulsion through celite and wash with ethyl acetate (3×100 mL). Separate the organics and dry over sodium sulfate. Remove the solvent under vacuum and chromatograph the product over silica gel using ethyl acetate/hexane (5-30%) to elute. This affords the title compound (5.7 g, 93%) as an off white solid: MS (ES+): 523 (M+H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07749992B2
출처 데이터셋uspto-grants-2010_07
ORD IDord-ad021bea2b2e41b897343e5b30b1b8ea
출처 메모uspto-grants-2010_07