4-Vinylpyridine → HCID 20339420, compound

HRID 1395447Notes

Reaction equation

HRID 1395447 reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][C:11]=1[Cl:12])[N:8]1[CH2:13][CH2:14][NH:15][CH2:16][CH:7]1[C:6](=[O:17])[NH:5]2.[CH:18]([C:20]1[CH:25]=[CH:24][N:23]=[CH:22][CH:21]=1)=[CH2:19]>>[Cl:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][C:11]=1[Cl:12])[N:8]1[CH2:13][CH2:14][N:15]([CH2:19][CH2:18][C:20]3[CH:25]=[CH:24][N:23]=[CH:22][CH:21]=3)[CH2:16][CH:7]1[C:6](=[O:17])[NH:5]2

Participants

3

Reactant 2

HCID 75024-VinylpyridineHCID 390689475704-24-4

Product 1

HCID 20339420HCID 20339420, compound

Procedure

Treatment of 8,9-dichloro-2,3,4,4a-tetrahydro-1H-pyrazino-[1,2-a]quinoxalin-5(6H)-one (3 g.) with 5.4 g. of 4-vinylpyridine in the manner described in Example 1 gave 2.2 g. of the title compound as the dihydrochloride salt, m.p. 266°-269° C. (dec.).

Workup

  1. customgave 2.2 g

Sources & evidence

ORD record
ord-b72af1611c8748f88555bd1c11bb5d26
Source dataset
uspto-grants-1980_05
Patent number
US04203987

Reaction notes

Loading…