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HRID 1727423생성일: 2026년 10월 26일

Hydrochloric Acid → 4-[(diisobutylamino)methyl]-N-(3-{methyl[2-(4-pyridinyl)ethyl]amino}propyl)-1,2-benzenediamine

https://huagongshe.com/reaction/1727423

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참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Ethyl AcetateHCID 8857—
반응물N,N-diisobutyl-4-({3-[methyl(2-pyridin-4-ylethyl)amino]propyl}amino)-3-nitrobenzamideHCID 69026668—
용매TetrahydrofuranHCID 8028—
생성물4-[(diisobutylamino)methyl]-N-(3-{methyl[2-(4-pyridinyl)ethyl]amino}propyl)-1,2-benzenediamineHCID 69028166—

반응 조건

온도0 °C

반응 단계

A molar solution of borane-tetrahydrofuran complex (6.25 ml, 15 eq) is added dropwise to a solution of N,N-diisobutyl-4-({3-[methyl(2-pyridin-4-ylethyl)amino]propyl}amino)-3-nitrobenzamide (200 mg, 1 eq) in tetrahydrofuran (3 ml) cooled down to 0° C. The mixture is heated under reflux for 20 hours then cooled down to 0° C. and hydrolysed with a 6N aqueous solution of hydrochloric acid (12 ml). After 1 hour 30 minutes under reflux, the mixture is cooled down to 0° C. and brought to basic pH by a 6N aqueous solution of soda. After adding ethyl acetate, decanting and extracting, the organic phases are combined, followed by washing with salt water, drying over sodium sulphate and evaporating under reduced pressure. Purification by flash chromatography on silica gel (eluent: 100% dichloromethane to dichloromethane/methanol 8:2) produces the expected compound in the form of an oil (92 mg, 51% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07495110B2
출처 데이터셋uspto-grants-2009_02
ORD IDord-a061309e876445ca8bdcb9ef592ff9cf
출처 메모uspto-grants-2009_02