돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 75157생성일: 2026년 10월 24일

Tricyclo(3.3.1.13,7)dec-1-ylmethylamine → HCID 59437175, 화합물

https://huagongshe.com/ko/reaction/75157

반응식

참여 물질

역할이름HCID투입량
반응물Tricyclo(3.3.1.13,7)dec-1-ylmethylamineHCID 86625—
반응물(S)-tert-butyl 2-(t-butyldimethylsilyloxymethyl)aziridine-1-carboxylateHCID 72525716—
용매DichloromethaneHCID 6344—
생성물HCID 59437175HCID 5943717542.5%

반응 단계

To a solution of (1-adamantylmethyl)amine (15 g, 52 mmol) in anhydrous CH2Cl2 (50 mL) was added tert-butyl 2-((tert-butyldimethylsilyloxy)methyl)aziridine-1-carboxylate (13 g, 78.3 mmol). The mixture was stirred for 10 min, the solvent was removed in vacuo and the residue was stirred at 40° C. for 5 h. The mixture was diluted with EtOAc (500 mL) and washed with water (100 mL),1N aq HCl (50 mL), satd aq NaHCO3 (50 ml) and brine (50 mL), and dried over MgSO4. The solution was concentrated to give a residue, which was purified by chromatography on silica gel to give (S)-tert-butyl 1-(tert-butyldimethylsilyloxy)-3-((1-adamantylmethyl)amino)propan-2-ylcarbamate (10 g, 24%). 1H NMR: (CDCl3, 400 MHz): δ=0.041 (s, 6H), 0.882 (s, 9H), 1.44 (s, 9H), 1.49 (s, 6H), 1.65 (m, 6H), 1.94 (s, 3H), 2.23 (s, 2H), 2.62-2.81 (m, 2H), 3.67 (m, 3H), 5.30 (s, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08835426B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-b12f6b0d30474bdbb69a09795a73ce18
출처 메모uspto-grants-2014_09