2-Indanone → HCID 66578319, compound

HRID 1529067Notes

Reaction equation

HRID 1529067 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.[CH2:15]1[C:23]2[C:18](=[CH:19][CH:20]=[CH:21][CH:22]=2)[CH2:17][C:16]1=O>>[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:16]2[CH2:15][C:23]3[C:18](=[CH:19][CH:20]=[CH:21][CH:22]=3)[CH2:17]2)=[CH:6][CH:7]=1

Participants

3

Reactant 2

HCID 119832-IndanoneHCID 582185375-(4-Bromophenyl)-3-methylisoxazol-4-amine

Product 1

HCID 66578319HCID 66578319, compound

Procedure

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

Workup

  1. customPrepared

Sources & evidence

ORD record
ord-7c7082d023cb45909835e8632208fbc8
Source dataset
uspto-grants-2015_07
Patent number
US09090573B2

Reaction notes

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