2-Aminomethyl-1-ethylpyrrolidine → HCID 15870689, compound

HRID 1637591Notes

Reaction equation

HRID 1637591 reaction equation
[CH2:1]([O:6][C:7]1[CH:15]=[CH:14][C:10]([C:11]([OH:13])=O)=[CH:9][CH:8]=1)[CH:2]=[C:3]([CH3:5])[CH3:4].[NH2:16][CH2:17][CH:18]1[CH2:22][CH2:21][CH2:20][N:19]1[CH2:23][CH3:24]>>[CH2:23]([N:19]1[CH2:20][CH2:21][CH2:22][CH:18]1[CH2:17][NH:16][C:11](=[O:13])[C:10]1[CH:9]=[CH:8][C:7]([O:6][CH2:1][CH:2]=[C:3]([CH3:4])[CH3:5])=[CH:15][CH:14]=1)[CH3:24]

Participants

3

Reactant 2

HCID 1172952-Aminomethyl-1-ethylpyrrolidineHCID 2671374-(3-methylbut-2-enoxy)benzoic acid

Product 1

HCID 15870689HCID 15870689, compoundYield 46%

Procedure

In a manner identical to Example 15, 4-prenyloxybenzoic acid(1.44 g) was subjected to a condensation reaction with 2-aminomethyl-1-ethylpyrrolidine (1.0 ml), thereby yielding 1.02 g(46%) of the aimed compound.

Sources & evidence

ORD record
ord-cbb17e65c62a44f8966b337ef39da7cc
Source dataset
uspto-grants-2000_03
Patent number
US06043243

Reaction notes

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