2-Aminomethyl-1-ethylpyrrolidine → HCID 15870688, compound

HRID 1637590Notes

Reaction equation

HRID 1637590 reaction equation
[CH2:1]([O:11][C:12]1[CH:20]=[CH:19][CH:18]=[CH:17][C:13]=1[C:14]([OH:16])=O)/[CH:2]=[C:3](/[CH2:5][CH2:6][CH:7]=[C:8]([CH3:10])[CH3:9])\[CH3:4].[NH2:21][CH2:22][CH:23]1[CH2:27][CH2:26][CH2:25][N:24]1[CH2:28][CH3:29]>>[CH2:28]([N:24]1[CH2:25][CH2:26][CH2:27][CH:23]1[CH2:22][NH:21][C:14](=[O:16])[C:13]1[CH:17]=[CH:18][CH:19]=[CH:20][C:12]=1[O:11][CH2:1]/[CH:2]=[C:3](/[CH2:5][CH2:6][CH:7]=[C:8]([CH3:9])[CH3:10])\[CH3:4])[CH3:29]

Participants

3

Reactant 2

HCID 1172952-Aminomethyl-1-ethylpyrrolidineHCID 53471241HCID 53471241, compound

Product 1

HCID 15870688HCID 15870688, compoundYield 80%

Procedure

In a manner identical to Example 15, 2-geranyloxybenzoic acid(1.37 g) was subjected to a condensation reaction with 2-aminomethyl-1-ethylpyrrolidine (0.7 ml), thereby yielding 1.53 g(80%) of the aimed compound.

Sources & evidence

ORD record
ord-eaf7bdbf979743439289790fb7e7edc5
Source dataset
uspto-grants-2000_03
Patent number
US06043243

Reaction notes

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