تفاعل #88512

ord-2aad88eff7364f1f9f9968439896e0fc

معادلة التفاعل

Fc1cc(Br)cnc1Cl
5-bromo-2-chloro-3-fluoropyridine
CC(C)(C)OC(N)=O
tert-butyl carbamate
O=C([O-])[O-].[Cs+].[Cs+]
cesium carbonate
CC(C)(C)OC(=O)Nc1cnc(Cl)c(F)c1
title compound
المردود 86.0%
CC(C)(C)OC(=O)Nc1cnc(Cl)c(F)c1
(6-Chloro-5-fluoropyridin-3-yl)-carbamic acid tert-butyl ester
المردود 86.0%

المذيبات

ظروف التفاعل

درجة الحرارة
85°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةThe reaction mixture was cooled to ambient temperature
  2. 2
    أخرىthe resultant solid was removed by filtration
  3. 3
    غسيلThe resultant solid was washed with ethyl acetate
  4. 4
    تركيزconcentrated in-vacuo
  5. 5
    أخرىto afford a residue that
  6. 6
    أخرىwas purified by flash chromatography (silica: cyclohexane to 25% ethyl acetate/cyclohexane)

الإجراء التجريبي

A degassed mixture of 5-bromo-2-chloro-3-fluoropyridine (22.5 g, 107 mmol), tert-butyl carbamate (13.8 g, 117.5 mmol), tris(dibenzylideneacetone) dipalladium(0) (2.95 g, 3.2 mmol), XantPhos (2.48 g, 4.28 mmol) and cesium carbonate (69.7 g, 214 mmol) in dioxane (340 mL) was heated at 85° C. for 24 hours. The reaction mixture was cooled to ambient temperature and the resultant solid was removed by filtration. The resultant solid was washed with ethyl acetate followed by dichloromethane and the filtrate was combined and concentrated in-vacuo to afford a residue that was purified by flash chromatography (silica: cyclohexane to 25% ethyl acetate/cyclohexane) to afford the title compound as a pale yellow solid (22.6 g, 86%). 1H NMR (300 MHz, CDCl3): 8.04 (dd, J=10.1, 2.4 Hz, 1H), 7.98 (d, J=2.4 Hz, 1H), 6.62 (s, 1H), 1.53 (s, 9H).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US09440976B2uspto-grants-2016_09