Isoindoline → HCID 57713895, compound

HRID 1984043Notes

Reaction equation

HRID 1984043 reaction equation
Cl[S:2]([C:5]1[CH:6]=[C:7]([CH:11]=[CH:12][C:13]=1[NH:14][CH3:15])[C:8]([OH:10])=[O:9])(=[O:4])=[O:3].[CH2:16]1[C:24]2[C:19](=[CH:20][CH:21]=[CH:22][CH:23]=2)[CH2:18][NH:17]1>>[CH2:16]1[C:24]2[C:19](=[CH:20][CH:21]=[CH:22][CH:23]=2)[CH2:18][N:17]1[S:2]([C:5]1[CH:6]=[C:7]([CH:11]=[CH:12][C:13]=1[NH:14][CH3:15])[C:8]([OH:10])=[O:9])(=[O:4])=[O:3]

Participants

3

Reactant 2

HCID 422478IsoindolineHCID 57713890HCID 57713890, compound

Product 1

HCID 57713895HCID 57713895, compound

Procedure

3-(Chlorosulfonyl)-4-(methylamino)benzoic acid 1.2 was reacted with isoindoline Ab following the procedure described in Example 1A. MS analysis (m−1)=331.

Sources & evidence

ORD record
ord-45fc84980c3a4b10a4bc1f7444f8a395
Source dataset
uspto-grants-2009_06
Patent number
US07544676B2

Reaction notes

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