Methyl 4-aminobutanoate → HCID 15124464, compound

HRID 1612886Notes

Reaction equation

HRID 1612886 reaction equation
[CH:1]([NH:3][CH:4]1[CH2:12][C:11]2[C:6](=[CH:7][CH:8]=[C:9]([CH2:13][C:14]([OH:16])=O)[CH:10]=2)[CH2:5]1)=[O:2].[NH2:17][CH2:18][CH2:19][CH2:20][C:21]([O:23][CH3:24])=[O:22]>>[CH:1]([NH:3][CH:4]1[CH2:12][C:11]2[C:6](=[CH:7][CH:8]=[C:9]([CH2:13][C:14]([NH:17][CH2:18][CH2:19][CH2:20][C:21]([O:23][CH3:24])=[O:22])=[O:16])[CH:10]=2)[CH2:5]1)=[O:2]

Participants

3

Reactant 2

HCID 18614Methyl 4-aminobutanoateHCID 15124409HCID 15124409, compound

Product 1

HCID 15124464HCID 15124464, compound

Procedure

In the same manner as described in Example 1-(1), (2-formylaminoindan-5-yl)acetic acid (2.20 g) and methyl γ-aminobutyrate are reacted to give methyl 4-[(2-formylaminoindan-5-yl)acetylamino]-n-butyrate (2.57 g).

Sources & evidence

ORD record
ord-f67737b93c3242b4b1cd34d5b9d1c3d9
Source dataset
uspto-grants-1993_03
Patent number
US05190975

Reaction notes

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