2-Aminomethyl-1-ethylpyrrolidine → HCID 15870694, compound

HRID 1637600Notes

Reaction equation

HRID 1637600 reaction equation
[CH2:1]([O:6][C:7]1[CH:8]=[C:9]([CH:13]=[C:14]([O:22][CH2:23][CH:24]=[C:25]([CH3:27])[CH3:26])[C:15]=1[O:16][CH2:17][CH:18]=[C:19]([CH3:21])[CH3:20])[C:10](O)=[O:11])[CH:2]=[C:3]([CH3:5])[CH3:4].[NH2:28][CH2:29][CH:30]1[CH2:34][CH2:33][CH2:32][N:31]1[CH2:35][CH3:36]>>[CH2:35]([N:31]1[CH2:32][CH2:33][CH2:34][CH:30]1[CH2:29][NH:28][C:10](=[O:11])[C:9]1[CH:8]=[C:7]([O:6][CH2:1][CH:2]=[C:3]([CH3:5])[CH3:4])[C:15]([O:16][CH2:17][CH:18]=[C:19]([CH3:21])[CH3:20])=[C:14]([O:22][CH2:23][CH:24]=[C:25]([CH3:27])[CH3:26])[CH:13]=1)[CH3:36]

Participants

3

Reactant 2

HCID 1172952-Aminomethyl-1-ethylpyrrolidineHCID 18799461HCID 18799461, compound

Product 1

HCID 15870694HCID 15870694, compoundYield 99.5%

Procedure

In a manner identical to Example 15, 3,4,5-triprenyloxybenzoic acid(0.94 g) was subjected to a condensation reaction with 2-aminomethyl-1-ethylpyrrolidine (0.35 g), thereby yielding 1.21 g(79%) of the aimed compound.

Sources & evidence

ORD record
ord-e004a105cd3644f8bc1b982a646b36fd
Source dataset
uspto-grants-2000_03
Patent number
US06043243

Reaction notes

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