반응 #1093000

ord-37fab5bceebc4ed0a16b9a0a082a504b

반응 방정식

CCCN1CCNCC1
1-propylpiperazine
COc1ccccc1Sc1ccc(-c2ccnc(Cl)c2)cc1C(F)(F)F
compound 96
COc1ccccc1Sc1ccc(-c2ccnc(Cl)c2)cc1C(F)(F)F
2-chloro-4-(4-(2-methoxy-phenylsulfanyl)-3-trifluoromethyl-phenyl)-pyridine
OC1CCNC1
3-hydroxypyrrolidine
CCCN1CCN(c2cc(-c3ccc(Sc4ccccc4OC)c(C(F)(F)F)c3)ccn2)CC1
solid 114
CCCN1CCN(c2cc(-c3ccc(Sc4ccccc4OC)c(C(F)(F)F)c3)ccn2)CC1
1-(4-(4-(2-Methoxy-phenylsulfanyl)-3-trifluoromethyl-phenyl)-pyridin-2-yl)-4-propyl-piperazine

반응 조건

상세 조건
See reaction.notes.procedure_details.

실험 절차

The title compound was prepared according to the procedures of Example 38E, substituting compound 76 with compound 96 (0.039 g, 0.0985 mmol) and 3-hydroxypyrrolidine with 1-propylpiperazine. A yellow solid 114 was obtained (0.033 g, 69%). 1H-NMR (CDCl3, 400 MHz) δ 1.03 (t, J=7.3 Hz, 3H), 1.83-1.92 (m, 2H), 2.65-3.10 (br, 8H), 2.98-3.04 (m, 2H), 3.83 (s, 3H), 6.89 (s, 1H), 6.99-7.06 (m, 3H), 7.09 (d, J=8.1 Hz, 1H), 7.43-7.52 (m, 3H), 7.85 (s, 1H), 8.26 (d, J=5.9 Hz, 1H); MS (APCI) m/z 488 (M+H)+.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US06787542B2uspto-grants-2004_09