Ethylenediamine → HCID 69421673, compound

HRID 1591762Notes

Reaction equation

HRID 1591762 reaction equation
[C:1]([C:3]1[CH:8]=[CH:7][C:6]([CH2:9][CH2:10][N:11]([CH2:30][CH3:31])[C:12](=[O:29])[CH2:13][CH2:14][CH2:15][NH:16][CH2:17][S:18]([C:21]2[CH:26]=[CH:25][CH:24]=[C:23]([Cl:27])[C:22]=2[Cl:28])(=[O:20])=[O:19])=[CH:5][CH:4]=1)#[N:2].[S].[CH2:33](N)[CH2:34][NH2:35]>>[Cl:28][C:22]1[C:23]([Cl:27])=[CH:24][CH:25]=[CH:26][C:21]=1[S:18]([CH2:17][NH:16][CH2:15][CH2:14][CH2:13][C:12]([N:11]([CH2:10][CH2:9][C:6]1[CH:5]=[CH:4][C:3]([C:1]2[NH:35][CH2:34][CH2:33][N:2]=2)=[CH:8][CH:7]=1)[CH2:30][CH3:31])=[O:29])(=[O:20])=[O:19]

Participants

4

Procedure

Analogously to 13b), 4-[(2,3-dichlorobenzenesulphonyl)methylamino]-N-{2-[4-(4,5-dihydro-1H-imidazol-2-yl)phenyl]ethyl}-N-ethylbutyramide was prepared from 0.74 g (1.53 mmol) of N-[2-(4-cyanophenyl)ethyl]-4-[(2,3-dichlorobenzenesulphonyl)methylamino]-N-ethylbutyramide, a spatula tip of sulphur and 5 ml of ethylenediamine.

Sources & evidence

ORD record
ord-baa4ee9c625e4cd9974972bbc4e9f472
Source dataset
uspto-grants-2007_11
Patent number
US07291642B2

Reaction notes

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