2-Aminomethyl-1-ethylpyrrolidine → HCID 70254859, compound

HRID 1637609Notes

Reaction equation

HRID 1637609 reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:9]=[C:10]([O:14][CH2:15]/[CH:16]=[C:17](/[CH2:19][CH2:20][CH:21]=[C:22]([CH3:24])[CH3:23])\[CH3:18])[C:11]=1[O:12][CH3:13])[C:6]([OH:8])=O.[NH2:25][CH2:26][CH:27]1[CH2:31][CH2:30][CH2:29][N:28]1[CH2:32][CH3:33]>>[CH2:32]([N:28]1[CH2:29][CH2:30][CH2:31][CH:27]1[CH2:26][NH:25][C:6](=[O:8])[C:5]1[CH:9]=[C:10]([O:14][CH2:15]/[CH:16]=[C:17](/[CH2:19][CH2:20][CH:21]=[C:22]([CH3:24])[CH3:23])\[CH3:18])[C:11]([O:12][CH3:13])=[C:3]([O:2][CH3:1])[CH:4]=1)[CH3:33]

Participants

3

Reactant 2

HCID 1172952-Aminomethyl-1-ethylpyrrolidineHCID 69853456HCID 69853456, compound

Product 1

HCID 70254859HCID 70254859, compoundYield 58.3%

Procedure

In a manner identical to Example 15, 3,4-dimethoxy-5-geranyloxy benzoic acid (0.80 g) was subjected to a condensation reaction with 2-aminomethyl-1-ethylpyrrolidine (0.31 g), thereby yielding 0.62 g(58%) of the aimed compound.

Sources & evidence

ORD record
ord-1171f7ed32bb4fe28ee2f0166234991b
Source dataset
uspto-grants-2000_03
Patent number
US06043243

Reaction notes

Loading…