تفاعل #324432

ord-1cb6e87a6de846118fb2db001002fd56

معادلة التفاعل

CCOC(=O)c1cc(CBr)oc1C(F)(F)F
title compound
CCOC(=O)c1cc(CBr)oc1C(F)(F)F
5-Bromomethyl-2-trifluoromethyl-furan-3-carboxylic acid ethyl ester
O=C([O-])[O-].[Cs+].[Cs+]
Cs2CO3
[Na+].[OH-]
NaOH
CC(C)(C)OC(=O)N1CC(Oc2cc(Cl)ccc2O)C1
3-(5-chloro-2-hydroxy-phenoxy)-azetidine-1-carboxylic acid tert-butyl ester
CC(C)(C)OC(=O)N1CC(Oc2cc(Cl)ccc2OCc2cc(C(=O)O)c(C(F)(F)F)o2)C1
title compound
CC(C)(C)OC(=O)N1CC(Oc2cc(Cl)ccc2OCc2cc(C(=O)O)c(C(F)(F)F)o2)C1
3-[2-(4-Carboxy-5-trifluoromethyl-furan-2-ylmethoxy)-5-chloro-phenoxy]-azetidine-1-carboxylic acid tert-butyl ester

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىThe title compound was prepared
  2. 2
    workup.ADDITIONwere added
  3. 3
    غسيلThe organic layer was washed with 1N NaOH
  4. 4
    أخرىdried
  5. 5
    أخرىThe crude material was purified by RP HPLC

الإجراء التجريبي

The title compound was prepared as described in Example 1 Step D using 3-(5-chloro-2-hydroxy-phenoxy)-azetidine-1-carboxylic acid tert-butyl ester (0.15 g, 0.50 mmol), the title compound of Step A (0.18 g, 0.60 mmol), Cs2CO3 (0.41 g, 1.2 mmol), KI (0.12 g, 0.70 mmol) in DMF, except upon completion of the reaction 1N NaOH and EtOAc were added. The organic layer was washed with 1N NaOH and dried. The crude material was purified by RP HPLC to provide the title compound. 1H NMR (CDCl3): 7.20-6.92 (m, 1H), 6.91-6.80 (m, 2H), 6.77-6.69 (m, 1H), 6.53 (d, J=2.1 Hz, 1H), 4.87 (s, 2H), 4.79-4.69 (m, 1H), 4.27-4.12 (m, 2H), 4.00-3.88 (m, 2H), 1.38 (s, 9H).

المصدر

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