2-Isopropoxy-5-methylsulfonylbenzoic acid → HCID 11619877, compound

HRID 2117438Notes

Reaction equation

HRID 2117438 reaction equation
[CH3:1][N:2]1[C:14]2[C:9](=[CH:10][CH:11]=[C:12]3[CH2:18][NH:17][CH2:16][CH2:15][C:13]3=2)[C:8]2[C:3]1=[CH:4][CH:5]=[CH:6][CH:7]=2.[CH:19]([O:22][C:23]1[CH:31]=[CH:30][C:29]([S:32]([CH3:35])(=[O:34])=[O:33])=[CH:28][C:24]=1[C:25](O)=[O:26])([CH3:21])[CH3:20]>>[CH:19]([O:22][C:23]1[CH:31]=[CH:30][C:29]([S:32]([CH3:35])(=[O:34])=[O:33])=[CH:28][C:24]=1[C:25]([N:17]1[CH2:16][CH2:15][C:13]2=[C:14]3[C:9](=[CH:10][CH:11]=[C:12]2[CH2:18]1)[C:8]1[C:3](=[CH:4][CH:5]=[CH:6][CH:7]=1)[N:2]3[CH3:1])=[O:26])([CH3:21])[CH3:20]

Participants

3

Reactant 2

HCID 211002372-Isopropoxy-5-methylsulfonylbenzoic acidHCID 68822078HCID 68822078, compound

Product 1

HCID 11619877HCID 11619877, compound

Procedure

Prepared in analogy to example 1.1 from 11-methyl-2,3,4,11-tetrahydro-1H-pyrido[4,3-a] carbazole and 2-isopropoxy-5-methanesulfonyl-benzoic acid (Example 2.1).

Sources & evidence

ORD record
ord-52b30f403eea4ef3b7a738ffd5fe0e27
Source dataset
uspto-grants-2008_10
Patent number
US07442710B2

Reaction notes

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