2-Acetylnaphthalene → HCID 66578229, compound

HRID 1528972Notes

Reaction equation

HRID 1528972 reaction equation
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[O:12][N:11]=[C:10]([CH3:13])[C:9]=2[NH2:14])=[CH:4][CH:3]=1.[CH:15]1[C:24]2[C:19](=[CH:20][CH:21]=[CH:22][CH:23]=2)[CH:18]=[CH:17][C:16]=1[C:25](=O)[CH3:26]>>[Br:1][C:2]1[CH:3]=[CH:4][C:5]([C:8]2[O:12][N:11]=[C:10]([CH3:13])[C:9]=2[NH:14][CH:25]([C:16]2[CH:17]=[CH:18][C:19]3[C:24](=[CH:23][CH:22]=[CH:21][CH:20]=3)[CH:15]=2)[CH3:26])=[CH:6][CH:7]=1

Participants

3

Reactant 2

HCID 71222-AcetylnaphthaleneHCID 582185375-(4-Bromophenyl)-3-methylisoxazol-4-amine

Product 1

HCID 66578229HCID 66578229, compound

Procedure

Prepared according to the procedure described in Example 24, Step 1, using 5-(4-bromo-phenyl)-3-methyl-isoxazol-4-ylamine and 1-naphthalen-2-yl-ethanone.

Workup

  1. customPrepared

Sources & evidence

ORD record
ord-9e7168f4e2b54fc79e84530b3e597d01
Source dataset
uspto-grants-2015_07
Patent number
US09090573B2

Reaction notes

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