2-(2-Bromoethyl)pyridine hydrobromide → 5-tert-Butyl-7-(3,3-difluoro-pyrrolidin-1-yl)-3-(2-pyridin-2-yl-ethyl)-3H-[1,2,3]triazolo[4,5-d]pyrimidine

반응식

[C:1]([C:5]1[N:6]=[C:7]([N:16]2[CH2:20][CH2:19][C:18]([F:22])([F:21])[CH2:17]2)[C:8]2[N:13]=[N:12][N:11]([CH2:14][CH3:15])[C:9]=2[N:10]=1)([CH3:4])([CH3:3])[CH3:2].C(C1N=[C:29]([N:36]2[CH2:40][CH2:39][C:38](F)(F)[CH2:37]2)C2N=NNC=2N=1)(C)(C)C.Br.BrCCC1C=CC=CN=1>>[C:1]([C:5]1[N:6]=[C:7]([N:16]2[CH2:20][CH2:19][C:18]([F:21])([F:22])[CH2:17]2)[C:8]2[N:13]=[N:12][N:11]([CH2:14][CH2:15][C:40]3[CH:39]=[CH:38][CH:37]=[CH:29][N:36]=3)[C:9]=2[N:10]=1)([CH3:2])([CH3:3])[CH3:4]

참가 물질

반응물 3

HCID 129138592-(2-Bromoethyl)pyridine hydrobromide

HCID 715582055-tert-Butyl-7-(3,3-difluoro-pyrrolidin-1-yl)-3-ethyl-3H-[1,2,3]triazolo[4,5-d]pyrimidine

HCID 178441789HCID 178441789, 화합물

생성물 1

HCID 715591295-tert-Butyl-7-(3,3-difluoro-pyrrolidin-1-yl)-3-(2-pyridin-2-yl-ethyl)-3H-[1,2,3]triazolo[4,5-d]pyrimidine

실험 절차

In analogy to the procedure described for the synthesis of 5-tert-butyl-7-(3,3-difluoropyrrolidin-1-yl)-3-ethyl-3H-[1,2,3]triazolo[4,5-d]pyrimidine (example 61), the title compound was prepared from 5-tert-butyl-7-(3,3-difluoropyrrolidin-1-yl)-3H-[1,2,3]triazolo[4,5-d]pyrimidine and 2-(2-bromoethyl)pyridine hydrobromide and isolated as colorless gum. MS(m/e): 387.4 (MH+).