Cinnamic Acid → HCID 20613774, compound

HRID 1840883Notes

Reaction equation

HRID 1840883 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.[C:12]1(/[CH:18]=[CH:19]/[C:20](O)=[O:21])[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1>>[N:3]12[CH2:10][CH2:9][CH:6]([CH2:7][CH2:8]1)[C@H:5]([NH:11][C:20](=[O:21])/[CH:19]=[CH:18]/[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)[CH2:4]2

Participants

3

Reactant 2

HCID 444539Cinnamic AcidHCID 12494973(3S)-1-azabicyclo[2.2.2]octan-3-amine dihydrochloride

Product 1

HCID 20613774HCID 20613774, compound

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-3-phenylpropenoic acid; MS (ES+) 257 (MH+).

Workup

  1. customPrepared as free base by a method analogous to

Sources & evidence

ORD record
ord-65c6deea8095429ba1ef07a3b3c2aa2f
Source dataset
uspto-grants-2004_01
Patent number
US06683090B1

Reaction notes

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