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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 883682생성일: 2026년 10월 26일

Ammonia → N,N-diisobutyl-1-{3-[methyl(2-pyridin-2-ylethyl)amino]propyl}-2-[(3,4,5-trimethoxyphenyl)amino]-1H-benzimidazole-5-carboxamide hydrochloride

https://huagongshe.com/reaction/883682

반응식

참여 물질

역할이름HCID투입량
반응물AmmoniaHCID 222—
반응물Hydrochloric AcidHCID 313—
반응물3,4,5-Trimethoxyphenyl isothiocyanateHCID 118900—
반응물3-amino-N,N-diisobutyl-4-({3-[methyl(2-pyridin-2-ylethyl)amino]propyl}amino)benzamideHCID 69026788—
용매Diethyl EtherHCID 3283—
용매TetrahydrofuranHCID 8028—
생성물N,N-diisobutyl-1-{3-[methyl(2-pyridin-2-ylethyl)amino]propyl}-2-[(3,4,5-trimethoxyphenyl)amino]-1H-benzimidazole-5-carboxamide hydrochlorideHCID 69029004—

반응 단계

3,4,5 trimethoxyphenylisothiocyanate (27 mg, 1.2 eq) and N-methylcyclohexylcarbodiimide-N-methyl-polystyrene resin (acquired from Novabiochem; load 1.69 mmol/g, 236 mg, 4 eq) are added successively to a solution of 3-amino-N,N-diisobutyl-4-({3-[methyl(2-pyridin-2-ylethyl)amino]propyl}amino) benzamide (48 mg, 1 eq) in tetrahydrofuran (2 ml). The mixture is heated under reflux for 18 hours then cooled down to ambient temperature and aminomethyl polystyrene resin (acquired from Novabiochem, 2 eq) is added. After stirring for 4 hours at ambient temperature, the mixture is filtered on frit and the filtrate is concentrated under reduced pressure at 40° C. The residue obtained is dissolved in ethyl ether and a solution of 1N HCl in ethyl ether is added dropwise in order to produce the expected compound in the form of the hydrochloride salt (80 mg, 89% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08236965B2
출처 데이터셋uspto-grants-2012_08
ORD IDord-eb0683ce06824d11a52c7523cf43050e
출처 메모uspto-grants-2012_08