HCID 5128704, compound → HCID 57445268, compound

HRID 2117436Notes

Reaction equation

HRID 2117436 reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][C:12]=1[O:13][CH3:14])[CH2:9][NH:8][CH2:7][C:6]2=[O:15].[CH:16]([O:19][C:20]1[CH:28]=[CH:27][C:26]([S:29]([CH3:32])(=[O:31])=[O:30])=[CH:25][C:21]=1[C:22](O)=[O:23])([CH3:18])[CH3:17]>>[CH:16]([O:19][C:20]1[CH:28]=[CH:27][C:26]([S:29]([CH3:32])(=[O:31])=[O:30])=[CH:25][C:21]=1[C:22]([N:8]1[CH2:7][C:6](=[O:15])[C:5]2[C:10](=[CH:11][C:12]([O:13][CH3:14])=[C:3]([O:2][CH3:1])[CH:4]=2)[CH2:9]1)=[O:23])([CH3:18])[CH3:17]

Participants

3

Reactant 2

HCID 5128704HCID 5128704, compoundHCID 211002372-Isopropoxy-5-methylsulfonylbenzoic acid

Product 1

HCID 57445268HCID 57445268, compound

Procedure

Prepared in analogy to example 1.1 from 6,7-dimethoxy-2,3-dihydro-1H-isoquinolin-4-one (CA [206763-75-9]) and 2-isopropoxy-5-methanesulfonyl-benzoic acid (Example 2.1). MS (m/e): 448.3 (M+H+).

Sources & evidence

ORD record
ord-ae9601dc6be045a2a78bcf9a9fa1bc60
Source dataset
uspto-grants-2008_10
Patent number
US07442710B2

Reaction notes

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