2,4,5-Trichloro-N-(2-chloroethyl)-N-isopropyl Benzene Sulfonamide → HCID 178457367, compound

HRID 431632Notes

Reaction equation

HRID 431632 reaction equation
[Cl:1][C:2]1[CH:7]=[C:6]([Cl:8])[C:5]([Cl:9])=[CH:4][C:3]=1[S:10]([N:13]([CH2:17][CH2:18]Cl)[CH:14]([CH3:16])[CH3:15])(=[O:12])=[O:11].[F:20][C:21]1[CH:35]=[CH:34][C:24]2[NH:25][C:26]([CH:28]3[CH2:33][CH2:32][NH:31][CH2:30][CH2:29]3)=[N:27][C:23]=2[CH:22]=1>>[Cl:1][C:2]1[CH:7]=[C:6]([Cl:8])[C:5]([Cl:9])=[CH:4][C:3]=1[S:10]([N:13]([CH2:17][CH2:18][N:31]1[CH2:30][CH2:29][CH:28]([C:26]2[NH:25][C:24]3[CH:34]=[CH:35][C:21]([F:20])=[CH:22][C:23]=3[N:27]=2)[CH2:33][CH2:32]1)[CH:14]([CH3:15])[CH3:16])(=[O:11])=[O:12]

Participants

3

Reactant 2

HCID 187615182,4,5-Trichloro-N-(2-chloroethyl)-N-isopropyl Benzene SulfonamideHCID 1785054646-Fluoro-2-(piperidin-4-yl)-1H-benzimidazole

Product 1

HCID 178457367HCID 178457367, compound

Procedure

The title compound was prepared using the procedure described in Example 1 using D7 and 4-(5-fluoro-1H-benzimidazol-2-yl)piperidine (D17). MH+ 547/549/551/553.

Sources & evidence

ORD record
ord-1c32f07947c44acf9975ccfc22768699
Source dataset
uspto-grants-2003_12
Patent number
US06660751B1

Reaction notes

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