HCID 67242907, compound → HCID 67242139, compound

HRID 2422009Notes

Reaction equation

HRID 2422009 reaction equation
C(OC([NH:8][CH2:9][CH2:10][C:11]([O:13][CH:14]1[CH2:19][CH2:18][N:17]([CH3:20])[CH2:16][CH2:15]1)=[O:12])=O)(C)(C)C.[ClH:21].NCCCC(OC1C(C)=CC=CC=1C)=O>>[ClH:21].[NH2:8][CH2:9][CH2:10][C:11]([O:13][CH:14]1[CH2:15][CH2:16][N:17]([CH3:20])[CH2:18][CH2:19]1)=[O:12]

Participants

3

Reactant 2

HCID 67242907HCID 67242907, compoundHCID 67244148HCID 67244148, compound

Product 1

HCID 67242139HCID 67242139, compound

Procedure

The title compound was prepared from 1-methylpiperidin-4-yl N-(tert-butoxycarbonyl)-β-alaninate in a similar manner as described for 2,6-dimethylphenyl 4-aminobutanoate hydrochloride. Mass Spectrum M+H+ 188.17.

Sources & evidence

ORD record
ord-f13a39c63048425d8b7d5a73ea54cdcb
Source dataset
uspto-grants-2011_06
Patent number
US07960380B2

Reaction notes

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