Allyl bromide → HCID 23323478, compound

HRID 1381124Notes

Reaction equation

HRID 1381124 reaction equation
[F:1][C:2]([F:20])([F:19])[O:3][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.[CH2:21](Br)[CH:22]=[CH2:23]>>[F:20][C:2]([F:1])([F:19])[O:3][C:4]1[CH:13]=[CH:12][C:11]2[N:10]([CH2:23][CH:22]=[CH2:21])[C:9](=[O:14])[N:8]3[CH2:15][CH2:16][CH2:17][N:18]=[C:7]3[C:6]=2[CH:5]=1

Participants

3

Reactant 2

HCID 7841Allyl bromideHCID 178517295HCID 178517295, compound

Product 1

HCID 23323478HCID 23323478, compound

Procedure

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

Sources & evidence

ORD record
ord-24d5ebbe0dd3451fb6d13185a1c46d9f
Source dataset
uspto-grants-1986_04
Patent number
US04585772

Reaction notes

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