1094303-23-7 → HCID 90408150, compound

HRID 2277559Notes

Reaction equation

HRID 2277559 reaction equation
[NH:1]1[CH:5]=[C:4]([C:6]2[CH:11]=[C:10]([C:12]#[N:13])[CH:9]=[CH:8][N:7]=2)[N:3]=[CH:2]1.Br[CH2:15][C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][C:17]=1[O:22][CH2:23][CH:24]([CH3:26])[CH3:25]>>[CH3:25][CH:24]([CH3:26])[CH2:23][O:22][C:17]1[CH:18]=[CH:19][CH:20]=[CH:21][C:16]=1[CH2:15][N:1]1[CH:5]=[C:4]([C:6]2[CH:11]=[C:10]([C:12]#[N:13])[CH:9]=[CH:8][N:7]=2)[N:3]=[CH:2]1

Participants

3

Reactant 2

HCID 431415621094303-23-7HCID 178510201HCID 178510201, compound

Product 1

HCID 90408150HCID 90408150, compound

Procedure

The title compound was prepared from 2-(1H-imidazol-4-yl)pyridine-4-carbonitrile (PREPARATION 4) and 1-(bromomethyl)-2-(2-methylpropoxyl)benzene according to the procedure for the preparation of Example 43, part A using room temp. [M+H] Calc'd for C20H20N4O, 333. Found, 333.

Sources & evidence

ORD record
ord-010c982737c0442380add6132f85a619
Source dataset
uspto-grants-2015_09
Patent number
US09133166B2

Reaction notes

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