alpha-Methylcinnamic acid → (S)-N-(1-Azabicyclo[2.2.2]oct-3-yl)(E-2-methyl-3-phenylpropenamide)

HRID 1840897Notes

Reaction equation

HRID 1840897 reaction equation
Cl.Cl.[N:3]12[CH2:10][CH2:9][CH:6]([CH2:7][CH2:8]1)[C@H:5]([NH2:11])[CH2:4]2.[CH3:12]/[C:13](=[CH:17]\[C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1)/[C:14](O)=[O:15]>>[N:3]12[CH2:10][CH2:9][CH:6]([CH2:7][CH2:8]1)[C@H:5]([NH:11][C:14](=[O:15])/[C:13](/[CH3:12])=[CH:17]/[C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1)[CH2:4]2

Participants

3

Procedure

Prepared as free base by a method analogous to that described in Example 1 from (S)-1-azabicyclo[2.2.2]oct-3-ylamine dihydrochloride and E-α-methyl-3-phenylpropenoic acid; MS (ES+) 271 (MH+).

Workup

  1. customPrepared as free base by a method analogous to

Sources & evidence

ORD record
ord-47087588acf9496f9ac60eaeb8b9ab3f
Source dataset
uspto-grants-2004_01
Patent number
US06683090B1

Reaction notes

Loading…