반응 #2446110

ord-03281f1d0d0d4dd3a2c2876651e5d3af

반응 방정식

O=C(NCCc1ccc(O)c(O)c1)C12CC3CC(C1)CC(c1ccc(Cl)cc1)(C3)C2
Compound 1
O=C(NCCc1ccc(O)c(O)c1)C12CC3CC(C1)CC(c1ccc(Cl)cc1)(C3)C2
3-(4-chlorophenyl)adamantane-1-carboxylic acid [2-(3,4-dihydroxyphenyl)ethyl]amide
CC(C)C(=O)Oc1cc(CCNC(=O)C23CC4CC(C2)CC(c2ccc(Cl)cc2)(C4)C3)ccc1O
Compound 5
CC(C)C(=O)Oc1cc(CCNC(=O)C23CC4CC(C2)CC(c2ccc(Cl)cc2)(C4)C3)ccc1O
isobutyric acid 5-(2-{[3-(4-chlorophenyl)adamantane-1-carbonyl]amino}ethyl)-2-hydroxyphenyl ester

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    농축The solution was then concentrated under a vacuum
  2. 2
    여과filtered

실험 절차

Compound 1 was dissolved in iso-butyric anhydride with a catalytic amount of 98% H2SO4 and stirred under N2 for 3 days at room temperature. The solution was then concentrated under a vacuum and filtered to give the product Compound 5, with a melting point of 126-128° C. 1H NMR (500 MHz, CDCl3) δ 1.29-1.33 (d, d, 6H, 2CH3), 1.74 (m, 2H, Admant-H), 1.81-1.88 (m, 8H, Admant-H), 1.94 (s, 2H, Admant-H), 2.26 (m, 2H, Admant-H), 2.74-2.81 (m, 2H, 2COCH), 2.82-2.85 (t, J=7.5 Hz, 2H, CH2), 3.50-3.54 (q, 2H, NCH2), 5.68 (s, 1H, NH), 6.99 (s, 1H, Ar—H), 7.05-7.07 (d, d, 1H, H—Ar), 7.11-7.13 (d, J=10 Hz, 1H, Ar—H), 7.30 (s, 4H, Ar—H); 13C NMR (500 MHz, CDCl3) δ 18.9, 28.8, 34.0, 35.0, 35.5, 36.5, 38.3, 40.3, 41.7, 42.0, 44.4, 123.5, 123.9, 126.4, 126.7, 128.3, 131.5, 137.7, 140.9, 142.2, 148.4, 174.4, 174.5, 177.4; MS m/z (relative intensity) 566.22 (MH+, 50), 567.22 (10), 567.22 (15).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08685936B2uspto-grants-2014_04