HCID 12264703, compound → HCID 57445265, compound

HRID 2117428Notes

Reaction equation

HRID 2117428 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([CH3:16])[CH3:15].[CH:17]([O:20][C:21]1[CH:29]=[CH:28][C:27]([S:30]([CH3:33])(=[O:32])=[O:31])=[CH:26][C:22]=1[C:23](O)=[O:24])([CH3:19])[CH3:18]>>[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][N:8]([C:23]([C:22]1[CH:26]=[C:27]([S:30]([CH3:33])(=[O:32])=[O:31])[CH:28]=[CH:29][C:21]=1[O:20][CH:17]([CH3:19])[CH3:18])=[O:24])[CH2:7][C:6]2([CH3:16])[CH3:15]

Participants

3

Reactant 2

HCID 12264703HCID 12264703, compoundHCID 211002372-Isopropoxy-5-methylsulfonylbenzoic acid

Product 1

HCID 57445265HCID 57445265, compound

Procedure

Prepared in analogy to example 1.1 from 6,7-dimethoxy-4,4-dimethyl-1,2,3,4-tetrahydro-isoquinoline (CA [57553-25-0]) and 2-isopropoxy-5-methanesulfonyl-benzoic acid (Example 2.1). MS (m/e): 462.5 (M+H+).

Sources & evidence

ORD record
ord-c6964352462f4e2f97ab778f69d82f88
Source dataset
uspto-grants-2008_10
Patent number
US07442710B2

Reaction notes

Loading…