Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Acetic Acid | HCID 176 | — |
| 반응물 | Methyl 4-oxoadamantane-1-carboxylate | HCID 4078246 | — |
| 반응물 | Sodium borohydride | HCID 4311764 | — |
| 반응물 | 2-(3-Chloro-phenyl)-propane-1,2-diamine | HCID 57495639 | — |
| 용매 | Ethanol | HCID 702 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | 4-[2-Amino-2-(3-chloro-phenyl)-propylamino]-adamantane-1-carboxylic acid methyl ester | HCID 57495640 | 86.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08129423B2 |
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| 출처 데이터셋 | uspto-grants-2012_03 |
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| ORD ID | ord-577800aa0fcd43729be1d65a83bb0007 |
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| 출처 메모 | uspto-grants-2012_03 |
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