5-Methoxy-1,2,3,4-tetrahydroisoquinoline → (2-Isopropoxy-5-methanesulfonyl-phenyl)-(5-methoxy-3,4-dihydro-1H-isoquinolin-2-yl)-methanone

HRID 2117437Notes

Reaction equation

HRID 2117437 reaction equation
[CH3:1][O:2][C:3]1[CH:12]=[CH:11][CH:10]=[C:9]2[C:4]=1[CH2:5][CH2:6][NH:7][CH2:8]2.[CH:13]([O:16][C:17]1[CH:25]=[CH:24][C:23]([S:26]([CH3:29])(=[O:28])=[O:27])=[CH:22][C:18]=1[C:19](O)=[O:20])([CH3:15])[CH3:14]>>[CH:13]([O:16][C:17]1[CH:25]=[CH:24][C:23]([S:26]([CH3:29])(=[O:28])=[O:27])=[CH:22][C:18]=1[C:19]([N:7]1[CH2:6][CH2:5][C:4]2[C:9](=[CH:10][CH:11]=[CH:12][C:3]=2[O:2][CH3:1])[CH2:8]1)=[O:20])([CH3:15])[CH3:14]

Participants

3

Reactant 2

HCID 139482495-Methoxy-1,2,3,4-tetrahydroisoquinolineHCID 211002372-Isopropoxy-5-methylsulfonylbenzoic acid

Product 1

HCID 58677889(2-Isopropoxy-5-methanesulfonyl-phenyl)-(5-methoxy-3,4-dihydro-1H-isoquinolin-2-yl)-methanone

Procedure

Prepared in analogy to example 1.1 from 5-methoxy-1,2,3,4-tetrahydro-isoquinoline (CA [103030-70-2]) and 2-isopropoxy-5-methanesulfonyl-benzoic acid (Example 2.1).

Sources & evidence

ORD record
ord-800a09be22114ddc9749abec782d9782
Source dataset
uspto-grants-2008_10
Patent number
US07442710B2

Reaction notes

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