4-[(Methylsulfonyl)amino]benzoyl chloride → HCID 19855923, compound

HRID 2073757Notes

Reaction equation

HRID 2073757 reaction equation
[CH3:1][CH:2]([C:4]1[CH:9]=[CH:8][CH:7]=[C:6]([CH:10]([CH3:12])[CH3:11])[C:5]=1[NH:13][CH2:14][CH2:15][N:16]([CH2:19][CH3:20])[CH2:17][CH3:18])[CH3:3].[CH3:21][S:22]([NH:25][C:26]1[CH:34]=[CH:33][C:29]([C:30]([Cl:32])=[O:31])=[CH:28][CH:27]=1)(=[O:24])=[O:23]>>[ClH:32].[CH2:17]([N:16]([CH2:19][CH3:20])[CH2:15][CH2:14][N:13]([C:5]1[C:6]([CH:10]([CH3:11])[CH3:12])=[CH:7][CH:8]=[CH:9][C:4]=1[CH:2]([CH3:1])[CH3:3])[C:30](=[O:31])[C:29]1[CH:33]=[CH:34][C:26]([NH:25][S:22]([CH3:21])(=[O:24])=[O:23])=[CH:27][CH:28]=1)[CH3:18]

Participants

3

Reactant 2

HCID 117911194-[(Methylsulfonyl)amino]benzoyl chlorideHCID 15057231HCID 15057231, compound

Product 1

HCID 19855923HCID 19855923, compound

Procedure

In a manner similar to Example I react N-[2,6-bis(1-methylethyl)phenyl]-N',N'-diethyl-1,2-ethanediamine with 4-[(methylsulfonyl)amino]benzoyl chloride to obtain the title compound.

Sources & evidence

ORD record
ord-0c2c3df9c3804ecea3a45619b8400a18
Source dataset
uspto-grants-1990_04
Patent number
US04920116

Reaction notes

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