Reacción #336840

ord-01ba197c4f6a4d3aa3f3bdac2f36daae

Ecuación de reacción

O=C(O)c1nc(C2CC2)nc(Cl)c1Cl
5,6-dichloro-2-cyclopropyl-4-pyrimidinecarboxylic acid
O=C(O)c1nc(C2CC2)nc(Cl)c1Cl
product
O=C(O)c1nc(C2CC2)nc(Cl)c1Cl
5,6-dichloro-2-cyclopropyl-4-pyrimidinecarboxylic acid
N
ammonia
Nc1nc(C2CC2)nc(C(=O)O)c1Cl
title product
Nc1nc(C2CC2)nc(C(=O)O)c1Cl
6-amino-5-chloro-2-cyclopropyl-4-pyrimidinecarboxylic acid

Disolventes

Condiciones de reacción

Temperatura
80°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    ConcentraciónThe solution was concentrated at 50° C.
  2. 2
    Otro70 torr (9.3 kPa) pressure to about half volume to remove most of the excess ammonia
  3. 3
    Temperaturacooled to 5° C.
  4. 4
    Filtraciónfiltered
  5. 5
    OtroThe isolated solid was dried in a vacuum oven

Procedimiento

A mixture of 5,6-dichloro-2-cyclopropyl-4-pyrimidinecarboxylic acid (i.e. the product of Step C1 or C2) (280 g, 1.2 mol), water (1.26 L) and aqueous ammonia (28%, 350 g, 5.76 mol) was heated at 80° C. for 5 h. The solution was concentrated at 50° C. and 70 torr (9.3 kPa) pressure to about half volume to remove most of the excess ammonia. The resulting slurry was stirred at 20° C., acidified to pH 1-2 with aqueous hydrochloric acid, cooled to 5° C. and filtered. The isolated solid was dried in a vacuum oven to afford the title product (270 g), a compound of the present invention.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07863220B2uspto-grants-2011_01