1-Bromopropane → HCID 15453540, compound

HRID 2185781Notes

Reaction equation

HRID 2185781 reaction equation
[CH3:1][O:2][C:3]([C:5]1[C:6](=[O:19])[NH:7][N:8]=[C:9]([C:11]2[CH:16]=[CH:15][C:14]([O:17][CH3:18])=[CH:13][CH:12]=2)[CH:10]=1)=[O:4].Br[CH2:21][CH2:22][CH3:23]>>[CH3:1][O:2][C:3]([C:5]1[C:6](=[O:19])[N:7]([CH2:21][CH2:22][CH3:23])[N:8]=[C:9]([C:11]2[CH:16]=[CH:15][C:14]([O:17][CH3:18])=[CH:13][CH:12]=2)[CH:10]=1)=[O:4]

Participants

3

Reactant 2

HCID 78401-BromopropaneHCID 15453537HCID 15453537, compound

Product 1

HCID 15453540HCID 15453540, compoundYield 78.3%

Procedure

Using 4-methoxycarbonyl-6-(4-methoxyphenyl)-2H-pyridazin-3-one and bromopropane as starting materials, the procedures of Example 1 were repeated likewise, whereby the title compound was obtained in a yield of 78.3%.

Sources & evidence

ORD record
ord-6c60f605bef44ddeb6a7f234ce4175cf
Source dataset
uspto-grants-2002_06
Patent number
US06403586B1

Reaction notes

Loading…