Bromomethyl 3-methoxyphenyl ketone → HCID 23003507, compound

HRID 396512Notes

Reaction equation

HRID 396512 reaction equation
[Cl:1][C:2]1[CH:13]=[CH:12][C:5](/[CH:6]=[CH:7]/[C:8]([O:10][CH3:11])=[O:9])=[C:4]([NH:14]S(C2C=CC=CC=2)(=O)=O)[CH:3]=1.[CH3:24][O:25][C:26]1[CH:27]=[C:28]([CH:33]=[CH:34][CH:35]=1)[C:29](=[O:32])[CH2:30]Br>>[CH3:11][O:10][C:8](=[O:9])[CH2:7][C:6]1[C:5]2[C:4](=[CH:3][C:2]([Cl:1])=[CH:13][CH:12]=2)[NH:14][C:30]=1[C:29](=[O:32])[C:28]1[CH:33]=[CH:34][CH:35]=[C:26]([O:25][CH3:24])[CH:27]=1

Participants

3

Reactant 2

HCID 101294Bromomethyl 3-methoxyphenyl ketoneHCID 11371593Methyl trans-4-chloro-2-(phenylsulfonylamino)cinnamate

Product 1

HCID 23003507HCID 23003507, compound

Procedure

The title compound was prepared according to the procedure described in Example 57 from methyl trans 4-chloro-2-(phenylsulfonylamino)cinnamate (step 1 of Example 8, Method A) and 3-methoxyphenacyl bromide.

Sources & evidence

ORD record
ord-fe812c8d424a4662b6d79778fb40b80f
Source dataset
uspto-grants-2003_08
Patent number
US06608070B1

Reaction notes

Loading…