反应 #336837

ord-e706e34adbfd42c5aa7543492c59f71d

反应方程式

N
ammonia
O=P(Cl)(Cl)Cl
Phosphorus oxychloride
O=C(O)c1nc(C2CC2)[nH]c(=O)c1Cl
5-chloro-2-cyclopropyl-1,6-dihydro-6-oxo-4-pyrimidinecarboxylic acid
O=C(O)c1nc(C2CC2)[nH]c(=O)c1Cl
product
O=C(O)c1nc(C2CC2)[nH]c(=O)c1Cl
5-chloro-2-cyclopropyl-1,6-dihydro-6-oxo-4-pyrimidine-carboxylic acid
O=C(O)c1nc(C2CC2)nc(Cl)c1Cl
title compound
O=C(O)c1nc(C2CC2)nc(Cl)c1Cl
5,6-dichloro-2-cyclopropyl-4-pyrimidinecarboxylic acid

反应条件

温度
85°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    温度The reaction mixture was cooled to 30° C.
  2. 2
    温度maintained at 5-10° C.
  3. 3
    浓缩the mixture was concentrated at 25° C. with a rotary evaporator
  4. 4
    其他to remove acetonitrile
  5. 5
    其他the precipitated product was isolated by filtration
  6. 6
    洗涤washed with water (2×25 mL)
  7. 7
    其他The solid was dried in a vacuum oven

实验过程

Phosphorus oxychloride (14 mL, 23 g, 0.15 mol) and 5-chloro-2-cyclopropyl-1,6-dihydro-6-oxo-4-pyrimidinecarboxylic acid (i.e. the product of Step B1 or B2) (75 g, 300 mmol) were combined and heated at 85° C. for 3 h. The reaction mixture was cooled to 30° C. and added over 30 minutes to a mixture of acetonitrile (50 mL) and ice water (80 mL), with the temperature maintained at 5-10° C. and the pH maintained in the range 1-3 by co-feeding aqueous ammonia (28%). The pH was adjusted to about 2, the mixture was concentrated at 25° C. with a rotary evaporator to remove acetonitrile, and the precipitated product was isolated by filtration and washed with water (2×25 mL). The solid was dried in a vacuum oven to afford the title compound (ca. 7.0 g).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07863220B2uspto-grants-2011_01