반응 #2122538

ord-bb613b9c988d4d0eba2f0784a9b00298

반응 방정식

O=C(O)C(F)(F)F
TFA
O=C(O)C(F)(F)F
TFA
c1c[nH]cn1
1b
c1c[nH]cn1
imidazole
c1c[nH]cn1
1b
c1c[nH]cn1
imidazole
[O-]B[O-]
1c
[O-]B[O-]
boronate
c1ccc(-c2ccccc2)cc1
Biphenyl

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타time=3 min, Flow rate=4 ml/min, Wavelength=220 nm, LC/MS (M+H)+=625.32

실험 절차

Example 1-4-d was prepared from 1-4-c and 1b in similar fashion to the preparation of 1d from 1b and 1c. 1H NMR (500 MHz, DMSO-d6) δ ppm 0.99-1.60 (m, 18 H) 1.75-2.11 (m, J=73.24 Hz, 6 H) 2.12-2.32 (m, 2 H) 3.32-3.41 (m, 2 H) 3.56 (s, 2 H) 4.63-5.02 (m, 2 H) 6.98-8.28 (m, 10 H) 11.67-12.33 (m, 2H); LC conditions: Phenomenex Luna 3.0×5.0 mm S10, Solvent A—0.1% TFA in 10% MeOH/90% H2O, Solvent B—0.1% TFA in 90% MeOH/10% H2O, 0 to 100% B over 2 min, Stop time=3 min, Flow rate=4 ml/min, Wavelength=220 nm, LC/MS (M+H)+=625.32. Retention time=1.438 min Additional Biphenyl Analogs were Prepared Similarly.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08574563B2uspto-grants-2013_11