2-Chloroquinoxaline → HCID 52919052, compound

HRID 1193152Notes

Reaction equation

HRID 1193152 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.[C:19]1([C:34]2[CH:39]=[CH:38][CH:37]=[CH:36][CH:35]=2)[CH:24]=[CH:23][CH:22]=[CH:21][C:20]=1[C:25]([N:27]1[CH2:33][CH:32]2[CH:29]([CH2:30][NH:31]2)[CH2:28]1)=[O:26].ClC1C=NC2C(=CC=CC=2)N=1>>[C:19]1([C:34]2[CH:39]=[CH:38][CH:37]=[CH:36][CH:35]=2)[CH:24]=[CH:23][CH:22]=[CH:21][C:20]=1[C:25]([N:27]1[CH2:33][CH:32]2[CH:29]([CH2:30][N:31]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)[CH2:28]1)=[O:26]

Participants

4

Reactant 3

HCID 2389382-ChloroquinoxalineHCID 671166512-(3,8-Diaza-bicyclo[4.2.0]oct-8-yl)-quinoxalineHCID 67116907HCID 67116907, compound

Product 1

HCID 52919052HCID 52919052, compound

Procedure

The title compound was prepared in a manner analogous to Intermediate 2, Step A, using Intermediate 19 and 2-chloro-quinoxaline. MS (ESI) mass calcd. for C26H22N4O, 406.49; m/z found, 407.2 [M+H]+.

Sources & evidence

ORD record
ord-5f38eacc53de40759b5619d710bfe7ad
Source dataset
uspto-grants-2014_03
Patent number
US08680275B2

Reaction notes

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