2,6-Octadiene, 1-bromo-3,7-dimethyl-, (2E)- → 2-Geranylthio-3-phenyl-4(3H)-quinazolinone

HRID 1085057Notes

Reaction equation

HRID 1085057 reaction equation
[SH:1][C:2]1[N:11]([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)[C:10](=[O:18])[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[N:3]=1.[CH2:19](Br)/[CH:20]=[C:21](/[CH2:23][CH2:24][CH:25]=[C:26]([CH3:28])[CH3:27])\[CH3:22]>>[CH2:19]([S:1][C:2]1[N:11]([C:12]2[CH:13]=[CH:14][CH:15]=[CH:16][CH:17]=2)[C:10](=[O:18])[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[N:3]=1)/[CH:20]=[C:21](/[CH2:23][CH2:24][CH:25]=[C:26]([CH3:28])[CH3:27])\[CH3:22]

Participants

3

Procedure

The title compound was prepared in a yield of 57.6%, using 2-mercapto-3-phenyl-4(3H)-quinazolinone in place of 3-isobutyl-2-mercapto-4(3H)-quinazolinone and geranyl bromide in place of 2-chloromethylpyridine hydrochloride.

Sources & evidence

ORD record
ord-cb15a5e092a044c4acb3859b227de677
Source dataset
uspto-grants-1991_04
Patent number
US05008266

Reaction notes

Loading…