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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 348631생성일: 2026년 10월 26일

Sodium Hydroxide → (4-{[bis(1H-imidazol-2-ylmethyl)-amino]-methyl}-phenyl)-[4-(1-propylbutyl)-piperazin-1-yl]-methanone

https://huagongshe.com/reaction/348631

반응식

참여 물질

역할이름HCID투입량
반응물Sodium HydroxideHCID 14798—
반응물4-HeptanoneHCID 31246—
반응물Sodium cyanoborohydrideHCID 5003444—
반응물(4-{[bis-(1H-imidazol-2-ylmethyl)-amino]-methyl}-phenyl)-piperazin-1-yl-methanoneHCID 21084462—
용매Acetic AcidHCID 176—
용매MethanolHCID 887—
용매TriethylamineHCID 8471—
생성물(4-{[bis(1H-imidazol-2-ylmethyl)-amino]-methyl}-phenyl)-[4-(1-propylbutyl)-piperazin-1-yl]-methanoneHCID 10344979—

반응 단계

The compound (57.7 mg) obtained in Example 32-2 was dissolved in methanol (1.73 ml) and then added with 4-heptanone (manufactured by Tokyo Kasei Kogyo Co., Ltd.) (30.7 μl), sodium cyanoborohydride (13.8 mg), and triethylamine (76.5 μl). The solution was adjusted to pH 5 with acetic acid and stirred at room temperature for 7 days. The reaction solution was added with a 1 mol/l sodium hydroxide aqueous solution and then the whole was separated and extracted with chloroform. The organic layer was dried with anhydrous sodium sulfate. The solvent was distilled off and the residue was then purified through silica gel column chromatography (chloroform/methanol) and treated with hydrochloric acid, thereby obtaining hydrochloride (27.7 mg) of the subject compound as a pale-yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07176227B2
출처 데이터셋uspto-grants-2007_02
ORD IDord-43763437075e4d34b69e9473346ee79c
출처 메모uspto-grants-2007_02