Benzenesulfonamide, 3-amino- → HCID 178509132, compound

HRID 255024Notes

Reaction equation

HRID 255024 reaction equation
[NH2:1][C:2]1[C:6](=[N:7][NH:8][C:9]2[CH:10]=[C:11](S(N)(=O)=O)[CH:12]=C[CH:14]=2)[C:5]([CH:19]2[CH2:21][CH2:20]2)=[N:4][N:3]=1.[NH2:22]C1C=C(S(N)(=O)=O)C=CC=1>>[CH:19]1([C:5]2[C:6](=[N:7][NH:8][C:9]3[CH:14]=[N:22][CH:12]=[CH:11][CH:10]=3)[C:2]([NH2:1])=[N:3][N:4]=2)[CH2:20][CH2:21]1

Participants

3

Reactant 2

HCID 7377Benzenesulfonamide, 3-amino-HCID 178509131HCID 178509131, compound

Product 1

HCID 178509132HCID 178509132, compound

Procedure

In a similar manner, 3-[N′-(3-amino-5-cyclopropylpyrazol-4-ylidene)hydrazino]benzenesulfonamide was prepared from 3-aminobenzenesulfonamide (0.51 g, 2.96 mmol) to yield 0.1 g of the product. MS (m/z, ES+): 307 (M+1, 100%).

Sources & evidence

ORD record
ord-9c246099dddd4ab38d830c2d9b334ee9
Source dataset
uspto-grants-2011_01
Patent number
US07875728B2

Reaction notes

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