تفاعل #324435

ord-2b8f0e302bb44ce79c0512a264b75a97

معادلة التفاعل

Cc1cc(CO)c(C(F)(F)F)o1
title compound
Cc1cc(CO)c(C(F)(F)F)o1
(5-Methyl-2-trifluoromethyl-furan-3-yl)-methanol
CC(C)(C)OC(=O)N1CC(Oc2cc(Cl)ccc2O)C1
3-(5-chloro-2-hydroxy-phenoxy)-azetidine-1-carboxylic acid tert-butyl ester
Cc1cc(COc2ccc(Cl)cc2OC2CN(C(=O)OC(C)(C)C)C2)c(C(F)(F)F)o1
3-[5-chloro-2-(5-methyl-2-trifluoromethyl-furan-3-ylmethoxy)-phenoxy]-azetidine-1-carboxylic acid tert-butyl ester

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

الإجراء التجريبي

Synthesized from the title compound of Step A and 3-(5-chloro-2-hydroxy-phenoxy)-azetidine-1-carboxylic acid tert-butyl ester using general procedure 7. MS (ESI): mass calcd. for C21H23ClF3NO5, 461.1; m/z found, 485.9 [M+Na]+. 1H NMR 6.91 (dd, J=8.6, 2.3 Hz, 1H), 6.84 (d, J=8.6 Hz, 1H), 6.55 (d, J=2.3 Hz, 1H), 6.22 (s, 1H), 5.07-5.00 (m, 2H), 4.90-4.81 (m, 1H), 4.30 (ddd, J=9.7, 6.5, 0.8 Hz, 2H), 4.06 (dd, J=9.8, 4.0 Hz, 2H), 2.34 (s, 3H), 1.45 (s, 9H).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08642583B2uspto-grants-2014_02