2-Naphthalenesulfonyl chloride → HCID 18180076, compound

HRID 2230138Notes

Reaction equation

HRID 2230138 reaction equation
[CH3:1][N:2]1[CH2:7][CH2:6][N:5]([C:8]2[CH:9]=[C:10]([NH2:14])[CH:11]=[CH:12][CH:13]=2)[CH2:4][CH2:3]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[S:25](Cl)(=[O:27])=[O:26]>>[CH3:1][N:2]1[CH2:3][CH2:4][N:5]([C:8]2[CH:9]=[C:10]([NH:14][S:25]([C:16]3[CH:17]=[CH:18][C:19]4[C:24](=[CH:23][CH:22]=[CH:21][CH:20]=4)[CH:15]=3)(=[O:27])=[O:26])[CH:11]=[CH:12][CH:13]=2)[CH2:6][CH2:7]1

Participants

3

Reactant 2

HCID 71252-Naphthalenesulfonyl chlorideHCID 115646133-(4-Methylpiperazin-1-yl)aniline

Product 1

HCID 18180076HCID 18180076, compound

Procedure

The title compound (E132) was prepared from 3-(4-methylpiperazin-1-yl)benzenamine and naphthalene-2-sulfonyl chloride according to the method of Example 1 MH+=382.

Sources & evidence

ORD record
ord-8e0b22c277f740f08a4e50d250583b6b
Source dataset
uspto-grants-2002_07
Patent number
US06423717B1

Reaction notes

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