2-Isopropoxy-5-methylsulfonylbenzoic acid → HCID 58677882, compound

HRID 2117425Notes

Reaction equation

HRID 2117425 reaction equation
[F:1][C:2]1[CH:19]=[CH:18][C:5]([CH2:6][O:7][C:8]2[CH:9]=[C:10]3[C:15](=[CH:16][CH:17]=2)[CH2:14][NH:13][CH2:12][CH2:11]3)=[CH:4][CH:3]=1.[CH:20]([O:23][C:24]1[CH:32]=[CH:31][C:30]([S:33]([CH3:36])(=[O:35])=[O:34])=[CH:29][C:25]=1[C:26](O)=[O:27])([CH3:22])[CH3:21]>>[F:1][C:2]1[CH:3]=[CH:4][C:5]([CH2:6][O:7][C:8]2[CH:9]=[C:10]3[C:15](=[CH:16][CH:17]=2)[CH2:14][N:13]([C:26]([C:25]2[CH:29]=[C:30]([S:33]([CH3:36])(=[O:35])=[O:34])[CH:31]=[CH:32][C:24]=2[O:23][CH:20]([CH3:22])[CH3:21])=[O:27])[CH2:12][CH2:11]3)=[CH:18][CH:19]=1

Participants

3

Reactant 2

HCID 211002372-Isopropoxy-5-methylsulfonylbenzoic acidHCID 22641899HCID 22641899, compound

Product 1

HCID 58677882HCID 58677882, compound

Procedure

Prepared in analogy to example 1.1 from 6-(4-fluoro-benzyloxy)-1,2,3,4-tetrahydro-isoquinoline (CA [620606-78-2]) and 2-isopropoxy-5-methanesulfonyl-benzoic acid (Example 2.1). MS (m/e): 498.4 (M+H+).

Sources & evidence

ORD record
ord-1eed14a7823645e5ad0ffbcbac697d90
Source dataset
uspto-grants-2008_10
Patent number
US07442710B2

Reaction notes

Loading…