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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 7158생성일: 2026년 10월 23일

Sodium triacetoxyborohydride → n-(3-Chloro-5-(trifluoromethyl)-2-pyridinylmethyl)-n'-(1h-benzimidazol-2-ylmethyl)-n'-(5,6,7,8-tetrahydro-8-quinolinyl)-1,4-benzenedimethanamine

https://huagongshe.com/ko/reaction/7158

반응식

참여 물질

역할이름HCID투입량
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물N-[(1H-Benzo[d]imidazol-2-yl)methyl]-N-(4-(aminomethyl)-benzyl)-5,6,7,8-tetrahydroquinolin-8-amineHCID 21985008—
반응물3-Chloro-5-(trifluoromethyl)picolinaldehydeHCID 22018790—
용매DichloromethaneHCID 6344—
생성물n-(3-Chloro-5-(trifluoromethyl)-2-pyridinylmethyl)-n'-(1h-benzimidazol-2-ylmethyl)-n'-(5,6,7,8-tetrahydro-8-quinolinyl)-1,4-benzenedimethanamineHCID 2201869026%

반응 단계

Using General Procedure B: To a stirred solution of N′-(1H-benzimidazol-2-ylmethyl)-N′-(5,6,7,8-tetrahydro-8-quinolinyl)-1,4-benzenedimethanamine (133 mg, 0.34 mmol) and 3-chloro-5-(trifluoromethyl)-pyridine-2-carboxaldehyde (66 mg, 0.32 mmol) in CH2Cl2 (5 mL) was added NaBH(OAc)3 (93 mg, 0.44 mmol) and the mixture was stirred at room temperature for 16 h. Purification of the crude material by radial chromatography on silica gel (1 mm plate, CH2Cl2/MeOH/NH4OH, 75:1:1) afforded the desired amine (48 mg, 26%) as a yellow foam.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07084155B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-a6b46ff1aa0f44429113e55ed89eb2bc
출처 메모uspto-grants-2006_08