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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 917349생성일: 2026년 10월 26일

Acetic Acid → N-(3-Cyano-6-{[1-(hydroxymethyl)-2,2-dimethylpropyl]amino}-4,5,6,7-tetrahydro-1-benzothien-2-yl)-2-ethylbutanamide

https://huagongshe.com/reaction/917349

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물2-Amino-3,3-dimethylbutan-1-olHCID 4149212—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물N-(3-Cyano-6-oxo-4,5,6,7-tetrahydro-1-benzothien-2-yl)-2-ethylbutanamideHCID 58962835—
용매DichloromethaneHCID 6344—
용매Sodium BicarbonateHCID 516892—
생성물N-(3-Cyano-6-{[1-(hydroxymethyl)-2,2-dimethylpropyl]amino}-4,5,6,7-tetrahydro-1-benzothien-2-yl)-2-ethylbutanamideHCID 58962825—

반응 단계

To a solution of the intermediate isolated in Example 9, Step C, in 40 mL of dichloromethane was added 0.452 g (3.90 mmol) of 2-amino-3,3-dimethylbutan-1-ol, followed by 1.24 g (5.9 mmol) of sodium triacetoxyborohydride and 0.468 mL (7.80 mmol) of acetic acid. After 16 h at ambient temperature the reaction was diluted with an equal volume of saturated aqueous NaHCO3. The organic layer was dried (Na2SO4) and concentrated in vacuo. Purification by preparative reversed phase HPLC afforded the title compound (TFA salt).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07273876B2
출처 데이터셋uspto-grants-2007_09
ORD IDord-caf7821ad0d54ab6abf035ce69687821
출처 메모uspto-grants-2007_09