Allyl bromide → HCID 23323491, compound

HRID 1381122Notes

Reaction equation

HRID 1381122 reaction equation
[N+:1]([C:4]1[CH:13]=[CH:12][C:11]2[NH:10][C:9](=[O:14])[N:8]3[CH2:15][CH2:16][CH2:17][N:18]=[C:7]3[C:6]=2[CH:5]=1)([O-:3])=[O:2].[CH2:19](Br)[CH:20]=[CH2:21]>>[N+:1]([C:4]1[CH:13]=[CH:12][C:11]2[N:10]([CH2:21][CH:20]=[CH2:19])[C:9](=[O:14])[N:8]3[CH2:15][CH2:16][CH2:17][N:18]=[C:7]3[C:6]=2[CH:5]=1)([O-:3])=[O:2]

Participants

3

Reactant 2

HCID 7841Allyl bromideHCID 178517282HCID 178517282, compound

Product 1

HCID 23323491HCID 23323491, compound

Procedure

Preparation analogously to Example 29 from 10-nitro-6-oxo-2,3,4,5,6,7-hexahydropyrimido-[1,2-c]-quinazoline and allyl bromide.

Sources & evidence

ORD record
ord-fa62059a388148fcaa27003e6fa11f00
Source dataset
uspto-grants-1986_04
Patent number
US04585772

Reaction notes

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