2-(2-Oxopyrrolidin-1-yl)acetic acid → HCID 53728295, compound

HRID 256379

Reaction equation

HRID 256379 reaction equation
[O:1]=[C:2]1[CH2:6][CH2:5][CH2:4][N:3]1[CH2:7][C:8]([OH:10])=O.[NH2:11][CH2:12][C:13]([N:15]1[CH:19]([CH3:20])[C:18](=[O:21])[NH:17][C:16]1([CH3:23])[CH3:22])=[O:14]>>[O:1]=[C:2]1[CH2:6][CH2:5][CH2:4][N:3]1[CH2:7][C:8]([NH:11][CH2:12][C:13]([N:15]1[CH:19]([CH3:20])[C:18](=[O:21])[NH:17][C:16]1([CH3:22])[CH3:23])=[O:14])=[O:10]

Participants

3

Reactant 2

HCID 31466872-(2-Oxopyrrolidin-1-yl)acetic acidHCID 201637481-(2-Aminoacetyl)-2,2,5-trimethyl-4-imidazolidinone

Product 1

HCID 53728295HCID 53728295, compound

Procedure

The same procedure of example 11, starting form 2-oxo-1-pyrrolidineacetic acid and 1-(2-aminoacetyl)-2,2,5-trimethyl-4-imidazolidinone, gave the title compound, m.p. 213°-215° C. dec.

Sources & evidence

ORD record
ord-d246e62b3a1f437ca910879e26708522
Source dataset
uspto-grants-1987_10
Patent number
US04703054

Linked notes

Loading…