반응 #70164

ord-c44f186e99ce41fc827f13d753c47952

반응 방정식

Fc1ccc(-c2cc3nc(Cl)nc(N4CCOCC4)c3s2)cn1
2-chloro-6-(6-fluoropyridin-3-yl)-4-morpholinothieno[3,2-d]pyrimidine
CCN(C(C)C)C(C)C
diisopropylethylamine
Nc1ccc(-c2cc3nc(Cl)nc(N4CCOCC4)c3s2)cn1
2-chloro-6-(6-aminopyridin-3-yl)-4-morpholinothieno[3,2-d]pyrimidine

반응 조건

온도
135°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타followed by removal of volatiles under high vacuum
  2. 2
    기타The crude mixture is purified by flash chromatography

실험 절차

A mixture of 2-chloro-6-(6-fluoropyridin-3-yl)-4-morpholinothieno[3,2-d]pyrimidine, about four equivalents of a primary or secondary amine (R═H, C1-C12 alkyl, C2-C8 alkenyl, C2-C8 alkynyl, C3-C12 carbocyclyl, C2-C20 heterocyclyl, C6-C20 aryl, or C1-C20 heteroaryl), and about two eq. diisopropylethylamine in N-methylpyrrolidine (˜0.1M) is heated to about 130-140° C. in a sealed microwave reactor for 10˜40 min, followed by removal of volatiles under high vacuum. The crude mixture is purified by flash chromatography to give intermediate 2-chloro-6-(6-aminopyridin-3-yl)-4-morpholinothieno[3,2-d]pyrimidine, which may be Suzuki coupled with a monocyclic heteroaryl, fused bicyclic heterocycle or heteroaryl boronate reagent following General Procedure A.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08536161B2uspto-grants-2013_09