HCID 19803566, compound → HCID 14306744, compound

HRID 1682062Notes

Reaction equation

HRID 1682062 reaction equation
[CH3:1][C:2]1[CH2:3][CH:4]2[C:9](=[CH:10][C:11]=1[CH3:12])[C:8](=[O:13])[NH:7][CH2:6][CH2:5]2.C1(C)C=CC(S(O[CH2:24][CH:25]2[CH2:29][CH2:28][N:27]([CH2:30][CH2:31][CH2:32][C:33]3[CH:42]=[CH:41][C:40]4[C:35](=[CH:36][CH:37]=[CH:38][CH:39]=4)[CH:34]=3)[CH2:26]2)(=O)=O)=CC=1>>[CH:34]1[C:35]2[C:40](=[CH:39][CH:38]=[CH:37][CH:36]=2)[CH:41]=[CH:42][C:33]=1[CH2:32][CH2:31][CH2:30][N:27]1[CH2:28][CH2:29][CH:25]([CH2:24][N:7]2[CH2:6][CH2:5][C:4]3[C:9](=[CH:10][C:11]([CH3:12])=[C:2]([CH3:1])[CH:3]=3)[C:8]2=[O:13])[CH2:26]1

Participants

3

Reactant 2

HCID 19803566HCID 19803566, compoundHCID 19804098HCID 19804098, compound

Product 1

HCID 14306744HCID 14306744, compound

Procedure

Prepared from 6,7-dimethyl-1-oxo-1,3,4,5-tetrahydro-isoquinoline and 3-(p-toluenesulphonyloxymethyl)-N-[3-(naphth-2-yl)-propyl]-pyrrolidine analogously to Example 2.

Sources & evidence

ORD record
ord-1355511ac10a4712822df9a2141e746e
Source dataset
uspto-grants-1992_12
Patent number
US05175157

Reaction notes

Loading…