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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 54852생성일: 2026년 10월 24일

2-adamantyloxycarbonyl-alpha-methyl-DL-tryptophan → Tricyclo [3.3.1.13,7]dec-2-yl (+/-)-[2-[[2-(3,4-dihydro-1-naphthalenyl)ethyl]amino]-1-(1H-indol-3-ylmethyl)-1-methyl-2-oxoethyl]carbamate

https://huagongshe.com/ko/reaction/54852

반응식

참여 물질

역할이름HCID투입량
반응물2-adamantyloxycarbonyl-alpha-methyl-DL-tryptophanHCID 14802503—
반응물3,4-Dihydro-1-naphthaleneethanamine hydrochlorideHCID 19047857—
생성물Tricyclo [3.3.1.13,7]dec-2-yl (+/-)-[2-[[2-(3,4-dihydro-1-naphthalenyl)ethyl]amino]-1-(1H-indol-3-ylmethyl)-1-methyl-2-oxoethyl]carbamateHCID 86747495—

반응 단계

Following the procedure of Example 70, the title compound was prepared from 0.50 g (1.26 mmol) of 2-adamantyloxycarbonyl-α- methyl-DL-tryptophan and 0.29 g (1.38 mmol) of 3,4-dihydro-1-naphthalene ethanamine hydrochloride. The purified product after chromatography was obtained as a white foam, 0.41 g (59%); 1H NMR (CDCl3) δ1.48-1.99 (17H, m), 2.39-2.50 (2H, m), 2.67-2.82 (3H, m), 3.23-3.57 (3H, m), 3.99 (2H, t, J 5.0 Hz), 4.84 (1H, br s), 5.24 (1H, br s), 5.73 (1H, m), 6.16 (1H, m), 7.00-7.63 (9H, m), 8.12 (1H, br s).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05622983
출처 데이터셋uspto-grants-1997_04
ORD IDord-5cbfd043e0054ec29ddfecea61e42edb
출처 메모uspto-grants-1997_04