Phenylsulphonyl isocyanate → HCID 66578370, compound

HRID 1528715Notes

Reaction equation

HRID 1528715 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.[C:15]1([S:21]([N:24]=[C:25]=[O:26])(=[O:23])=[O:22])[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1>>[C:15]1([S:21]([NH:24][C:25]([NH:14][C:9]2[C:10]([CH3:13])=[N:11][O:12][C:8]=2[C:5]2[CH:4]=[CH:3][C:2]([Br:1])=[CH:7][CH:6]=2)=[O:26])(=[O:22])=[O:23])[CH:16]=[CH:17][CH:18]=[CH:19][CH:20]=1

Participants

3

Reactant 2

HCID 76096Phenylsulphonyl isocyanateHCID 582185375-(4-Bromophenyl)-3-methylisoxazol-4-amine

Product 1

HCID 66578370HCID 66578370, compound

Procedure

Prepared according to the procedure described in Example 3, Step 7, using 5-(4-bromo-phenyl)-3-methyl-isoxazol-4-ylamine and benzenesulfonyl isocyanate.

Workup

  1. customPrepared

Sources & evidence

ORD record
ord-f39f172f62d14d869271290e695eae30
Source dataset
uspto-grants-2015_07
Patent number
US09090573B2

Reaction notes

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