2-Aminomethyl-1-ethylpyrrolidine → HCID 70254836, compound

HRID 1637608Notes

Reaction equation

HRID 1637608 reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:9]=[C:10]([O:23][CH3:24])[C:11]=1[O:12][CH2:13]/[CH:14]=[C:15](/[CH2:17][CH2:18][CH:19]=[C:20]([CH3:22])[CH3:21])\[CH3:16])[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:23][CH3:24])[C:11]([O:12][CH2:13]/[CH:14]=[C:15](/[CH2:17][CH2:18][CH:19]=[C:20]([CH3:22])[CH3:21])\[CH3:16])=[C:3]([O:2][CH3:1])[CH:4]=1)[CH3:33]

Participants

3

Reactant 2

HCID 1172952-Aminomethyl-1-ethylpyrrolidineHCID 69853474HCID 69853474, compound

Product 1

HCID 70254836HCID 70254836, compoundYield 95.9%

Procedure

In a manner identical to Example 15, 3,5-dimethoxy-4-geranyloxy benzoic acid (0.80 g) was subjected to a condensation reaction with 2-aminomethyl-1-ethylpyrrolidine (0.31 g), thereby yielding 1.02 g(95%) of the aimed compound.

Sources & evidence

ORD record
ord-71e755c613dd4c928b7c986a497cc1bd
Source dataset
uspto-grants-2000_03
Patent number
US06043243

Reaction notes

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