HRID2262168

反应详情

EQUATION

反应方程式

HRID 2262168 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
-78 °C

PROCEDURE

实验过程

2-Chloro-4-morpholinothieno[3,2-d]pyrimidine 4 (2.5 g) was cooled to −78° C. in 50 mL of THF before adding 1.3 eq of a 2.5M solution of nBuLi in hexanes. The reaction was stirred at −78° C. for 30 minutes before warming to −40° C. for several minutes to allow for complete formation of the Lithium anion. The reaction was then re-cooled to −78° C. and carbon dioxide gas evolved from dry ice was bubbled in via cannula to the reaction solution for 1 hour. The reaction was then slowly warmed to 0° C. over 30 minutes and the THF was concentrated by rotovap. The reaction was then quenched with water and extracted with Ethyl Acetate to remove any 2-chloro-4-morpholinothieno[3,2-d]pyrimidine. The aqueous layer was then brought to pH of 2-3 by adding concentrated HCl. The resultant solid that crashed out of the aqueous layer was then collected by Buchner funnel, rinsed with water and dried overnight under vacuum to yield 2.65 g of 2-chloro-4-morpholinothieno[3,2-d]pyrimidine-6-carboxylic acid. 500 mg of this intermediate was then subjected to Procedure A. Upon extraction into Ethyl Acetate, the product remains in the aqueous layer and is treated with 20 eq of Amberlite IR-120 ion-exchange resin for 2 hours or until the solution becomes cloudy. The solution is first filtered thru a coarse Filter Flask to remove the resin and is then filtered thru a Buchner funnel to collect the 637 mg of 2-(1H-indazol-4-yl)-4-morpholinothieno[3,2-d]pyrimidine-6-carboxylic acid 13 as a light brown solid.

WORKUP

后处理

  1. temperaturebefore warming to −40° C. for several minutes
  2. temperatureThe reaction was then re-cooled to −78° C.
  3. customwas bubbled in via cannula to the reaction solution for 1 hour
  4. temperatureThe reaction was then slowly warmed to 0° C. over 30 minutes
  5. concentrationthe THF was concentrated by rotovap
  6. customThe reaction was then quenched with water
  7. extractionextracted with Ethyl Acetate
  8. customto remove any 2-chloro-4-morpholinothieno[3,2-d]pyrimidine
  9. additionby adding concentrated HCl
  10. customwas then collected by Buchner funnel
  11. washrinsed with water
  12. customdried overnight under vacuum