Methyl 4-aminobutanoate → HCID 15124466, compound

HRID 1612887Notes

Reaction equation

HRID 1612887 reaction equation
[CH2:1]([O:8][C:9]([NH:11][CH:12]1[CH2:20][C:19]2[C:14](=[CH:15][CH:16]=[C:17]([CH2:21][C:22](O)=[O:23])[CH:18]=2)[CH2:13]1)=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[NH2:25][CH2:26][CH2:27][CH2:28][C:29]([O:31][CH3:32])=[O:30]>>[CH2:1]([O:8][C:9]([NH:11][CH:12]1[CH2:20][C:19]2[C:14](=[CH:15][CH:16]=[C:17]([CH2:21][C:22]([NH:25][CH2:26][CH2:27][CH2:28][C:29]([O:31][CH3:32])=[O:30])=[O:23])[CH:18]=2)[CH2:13]1)=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

Participants

3

Reactant 2

HCID 18614Methyl 4-aminobutanoateHCID 15124500HCID 15124500, compound

Product 1

HCID 15124466HCID 15124466, compound

Procedure

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

Sources & evidence

ORD record
ord-bd458729a1b042fd8aa52278e828029e
Source dataset
uspto-grants-1993_03
Patent number
US05190975

Reaction notes

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