HRID253405
反应详情
EQUATION
反应方程式
REACTANTS
反应物
HCID9222
1H-Pyrrolo[2,3-b]pyridine
C7H6N2
HCID67709
1,1,1-Trifluoro-2-iodoethane
C2H2F3I
HCID69804
Ethane, 1-fluoro-2-iodo-
C2H4FI
HCID2736551
1-(bromomethyl)-4-chloro-2-fluorobenzene
C7H5BrClF
HCID3041214
4-Ethyl-2-[(4-methoxyphenyl)methyl]-4,5-dihydro-1,3-oxazole
C13H17NO2
HCID10307871
5-Methoxy-7-azaindole
C8H8N2O
PRODUCTS
生成物
PROCEDURE
实验过程
were prepared following the protocol of Scheme 20, substituting iodoethane with iodomethane in Step 3 to provide P-1891, or substituting iodoethane with 2-iodo-1,1,1-trifluoroethane in Step 3 to provide P-2076, or substituting iodoethane with 2-iodo-1-fluoroethane in Step 3 to provide P-2118, or substituting 4-chlorobenzyl bromide 22 with 4-chloro-2-fluoro-benzyl bromide in Step 1 and 7-azaindole 6 with 5-methoxy-7-azaindole in Step 4 to provide P-2016. MS (ESI) [M+H+]+=393.4 (P-1891), 461.08 (P-2076), 455.2 (P-2016), and 425.17 (P-2118).
WORKUP
后处理
- customto provide P-2076
- customto provide P-2118
- customto provide P-2016