Реакция #1563956

ord-b7d308467b1a4a14bded6c56adb5f110

Уравнение реакции

Fc1cc2c(c(C3CCCN3)c1)OCCO2
2-(7-fluoro-2,3-dihydrobenzo[b][1,4]dioxin-5-yl)pyrrolidine
CCOC(=O)c1cnn2ccc(Br)cc12
Ethyl 5-bromopyrazolo[1,5-a]pyridine-3-carboxylate
CCOC(=O)c1cnn2ccc(N3CCCC3c3cc(F)cc4c3OCCO4)cc12
title compound
CCOC(=O)c1cnn2ccc(N3CCCC3c3cc(F)cc4c3OCCO4)cc12
Ethyl 5-(2-(7-fluoro-2,3-dihydrobenzo[b][1,4]dioxin-5-yl)pyrrolidin-1-yl)pyrazolo[1,5-a]pyridine-3-carboxylate

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Другоеto afford as pale brown solid

Методика

The title compound (Int-65) was prepared by the method similar to that of Int-84 using 2-(7-fluoro-2,3-dihydrobenzo[b][1,4]dioxin-5-yl)pyrrolidine (Int-56B)) and Ethyl 5-bromopyrazolo[1,5-a]pyridine-3-carboxylate to afford as pale brown solid. LCMS (ESI): m/z 412.85 (M+H).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US09402833B2uspto-grants-2016_08