반응 #3555

ord-f181ec7fa91846eca2529e969dd97cf0

반응 방정식

Nc1ncc2cc(-c3c(F)cccc3F)c(N)nc2n1
6-(2,6-difluoro-phenyl)-pyrido[2,3-d]pyrimidine-2,7-diamine
Nc1ncc2cc(-c3c(F)cccc3F)c(N)nc2n1
6-(2,6-Difluoro-phenyl)-pyrido[2,3-d]pyrimidine-2,7-diamine
CC(C)(C)N=C=O
tert-butyl isocyanate
N
ammonia
CC(C)(C)NC(=O)Nc1nc2nc(N)ncc2cc1-c1c(F)cccc1F
title compound
CC(C)(C)NC(=O)Nc1nc2nc(N)ncc2cc1-c1c(F)cccc1F
1-[2-Amino-6-(2,6-difluoro-phenyl)-pyrido[2,3-d]pyrimidin-7-yl]-3-tert-butyl-urea

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타The product was purified by MPLC
  2. 2
    세척eluting with a gradient of CHCl3 :EtOAc (1:1) to EtOAc
  3. 3
    기타to afford the pure product

실험 절차

The title compound was prepared from 0.25 g of 6-(2,6-difluoro-phenyl)-pyrido[2,3-d]pyrimidine-2,7-diamine from Example 63 and 0.112 mL of tert-butyl isocyanate according to Example 2. The product was purified by MPLC eluting with a gradient of CHCl3 :EtOAc (1:1) to EtOAc to afford the pure product; mp >300° C., CIMS (1% ammonia in methane): m/z (relative intensity) 373 (MH+ +1, 60), 374 (MH+ +2, 10), 274 (100).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05733913uspto-grants-1998_03