5-Chlorovaleryl chloride → N-[5-(5-chloropentanoyl)-2,3-dihydro-1H-inden-2-yl]methanesulfonamide

HRID 2374616

Reaction equation

HRID 2374616 reaction equation
[CH2:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH2:3][CH:2]1[NH:10][S:11]([CH3:14])(=[O:13])=[O:12].[Cl:15][CH2:16][CH2:17][CH2:18][CH2:19][C:20](Cl)=[O:21]>>[Cl:15][CH2:16][CH2:17][CH2:18][CH2:19][C:20]([C:6]1[CH:5]=[C:4]2[C:9](=[CH:8][CH:7]=1)[CH2:1][CH:2]([NH:10][S:11]([CH3:14])(=[O:13])=[O:12])[CH2:3]2)=[O:21]

Participants

3

Reactant 2

HCID 740895-Chlorovaleryl chlorideHCID 21887329N-(2,3-dihydro-1H-inden-2-yl)methanesulfonamide

Product 1

HCID 21887757N-[5-(5-chloropentanoyl)-2,3-dihydro-1H-inden-2-yl]methanesulfonamide

Procedure

Using N-(2,3-dihydro-1H-inden-2-yl)methanesulfonamide and 5-chlorovaleryl chloride according to the same method as that of Example 1, the title compound was obtained as colorless crystals.

Sources & evidence

ORD record
ord-08ef191f2c5f4b01b223e4107ecfc957
Source dataset
uspto-grants-2008_12
Patent number
US07462628B2

Linked notes

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