Gamma-Aminobutyric Acid → HCID 2940027, compound

HRID 2105929Notes

Reaction equation

HRID 2105929 reaction equation
[CH:1]1[CH:10]=[C:9]2[C:11]([O:13][C:14](=[O:15])[C:7]3=[C:8]2[C:3](=[CH:4][C:5]([N+:16]([O-:18])=[O:17])=[CH:6]3)[CH:2]=1)=O.[NH2:19][CH2:20][CH2:21][CH2:22][C:23]([OH:25])=[O:24]>C(O)(=O)C>[N+:16]([C:5]1[CH:4]=[C:3]2[CH:2]=[CH:1][CH:10]=[C:9]3[C:8]2=[C:7]([CH:6]=1)[C:14](=[O:15])[N:19]([CH2:20][CH2:21][CH2:22][C:23]([OH:25])=[O:24])[C:11]3=[O:13])([O-:18])=[O:17]

Participants

4

Reactant 2

HCID 119Gamma-Aminobutyric AcidHCID 18194Naphthalic anhydride, 3-nitro-

Product 1

HCID 2940027HCID 2940027, compound

Reagents, catalysts & solvents 1

HCID 176Acetic AcidSolvent

Procedure

The compound was prepared from 3-nitro-1,8-naphthalic anhydride (1.00 g, 4.1 mmol) and 4-aminobutyric acid (0.42 g, 4.1 mmol) in 100 mL glacial acetic acid using the general procedure shown in Example 1.

Sources & evidence

ORD record
ord-c3a662c4597b438e836e982afebb9690
Source dataset
uspto-grants-2009_08
Patent number
US07579468B2

Reaction notes

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