2-Chloroquinoxaline → HCID 52919179, compound

HRID 1193156Notes

Reaction equation

HRID 1193156 reaction equation
C12N([C:9]3[CH:18]=[N:17][C:16]4[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=4)[N:10]=3)CC1CCNC2.[CH:19]12[CH2:25][NH:24][CH:23]1[CH2:22][N:21]([C:26]([C:28]1[CH:33]=[CH:32][CH:31]=[CH:30][C:29]=1[O:34][CH3:35])=[O:27])[CH2:20]2.ClC1C=NC2C(=CC=CC=2)N=1>>[CH3:35][O:34][C:29]1[CH:30]=[CH:31][CH:32]=[CH:33][C:28]=1[C:26]([N:21]1[CH2:22][CH:23]2[CH:19]([CH2:25][N:24]2[C:9]2[CH:18]=[N:17][C:16]3[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=3)[N:10]=2)[CH2:20]1)=[O:27]

Participants

4

Reactant 3

HCID 2389382-ChloroquinoxalineHCID 67116634HCID 67116634, compoundHCID 671166512-(3,8-Diaza-bicyclo[4.2.0]oct-8-yl)-quinoxaline

Product 1

HCID 52919179HCID 52919179, compound

Procedure

The title compound was prepared in a manner analogous to Intermediate 2, Step A, using Intermediate 22 and 2-chloro-quinoxaline as staring materials. MS (ESI) mass calcd. for O21H20N4O2, 360.42; m/z found, 361.3 [M+H]+.

Sources & evidence

ORD record
ord-7db7daaeeb17428b9b8a5b236cb0b71b
Source dataset
uspto-grants-2014_03
Patent number
US08680275B2

Reaction notes

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