2-Aminomethyl-1-ethylpyrrolidine → HCID 53799437, compound

HRID 1637593Notes

Reaction equation

HRID 1637593 reaction equation
[CH2:1]([O:6][C:7]1[CH:15]=[CH:14][C:13]([O:16][CH2:17][CH:18]=[C:19]([CH3:21])[CH3:20])=[CH:12][C:8]=1[C:9]([OH:11])=O)[CH:2]=[C:3]([CH3:5])[CH3:4].[NH2:22][CH2:23][CH:24]1[CH2:28][CH2:27][CH2:26][N:25]1[CH2:29][CH3:30]>>[CH2:29]([N:25]1[CH2:26][CH2:27][CH2:28][CH:24]1[CH2:23][NH:22][C:9](=[O:11])[C:8]1[CH:12]=[C:13]([O:16][CH2:17][CH:18]=[C:19]([CH3:21])[CH3:20])[CH:14]=[CH:15][C:7]=1[O:6][CH2:1][CH:2]=[C:3]([CH3:4])[CH3:5])[CH3:30]

Participants

3

Reactant 2

HCID 1172952-Aminomethyl-1-ethylpyrrolidineHCID 18799481HCID 18799481, compound

Product 1

HCID 53799437HCID 53799437, compoundYield 70%

Procedure

In a manner identical to Example 15, 2,5-diprenyloxybenzoic acid(1.45 g) was subjected to a condensation reaction with 2-aminomethyl-1-ethylpyrrolidine (0.7 ml), thereby yielding 1.40 g(70%) of the aimed compound.

Sources & evidence

ORD record
ord-578e8d3674024303a9cd91bc2edaa828
Source dataset
uspto-grants-2000_03
Patent number
US06043243

Reaction notes

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