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HRID 1092361생성일: 2026년 10월 27일

Acetic Acid → 4-[2-Amino-2-(3-chloro-phenyl)-propylamino]-adamantane-1-carboxylic acid methyl ester

https://huagongshe.com/reaction/1092361

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Methyl 4-oxoadamantane-1-carboxylateHCID 4078246—
반응물Sodium borohydrideHCID 4311764—
반응물2-(3-Chloro-phenyl)-propane-1,2-diamineHCID 57495639—
용매EthanolHCID 702—
용매WaterHCID 962—
생성물4-[2-Amino-2-(3-chloro-phenyl)-propylamino]-adamantane-1-carboxylic acid methyl esterHCID 5749564086.5%

반응 조건

온도0 °C

반응 단계

To a solution of 2-(3-chloro-phenyl)-propane-1,2-diamine (3.4 g) and 4-oxo-adamantane-1-carboxylic acid methyl ester (CAS 56674-88-5, 3.85 g) in ethanol (50 mL) was added acetic acid (0.7 mL) and reaction mixture was refluxed for 4 h, after which it was cooled to 0° C. and NaBH4 was added. The reaction mixture was then slowly brought to room temperature and left at stirring for 17 h. The reaction was monitored by TLC. After completion, water (30 mL) was slowly added. The reaction mixture was concentrated at reduced pressure to remove the ethanol. The aqueous layer was extracted with DCM (3×50 mL) and the organic layers were then dried over Na2SO4 and then concentrated to get crude desired 4-[2-amino-2-(3-chloro-phenyl)-propylamino]-adamantane-1-carboxylic acid methyl ester (6 g) as a mixture of E/Z isomers. The compound was used in the next step without further purification. MS (ESI): 377.4 (MH+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08129423B2
출처 데이터셋uspto-grants-2012_03
ORD IDord-577800aa0fcd43729be1d65a83bb0007
출처 메모uspto-grants-2012_03