2-Chloroquinoxaline → HCID 67090637, compound

HRID 2113513Notes

Reaction equation

HRID 2113513 reaction equation
C([O:5][C:6]([N:8]1[CH2:13][CH2:12][CH2:11][CH2:10][CH:9]1[CH2:14][NH2:15])=[O:7])(C)(C)C.Cl[C:17]1[CH:26]=[N:25][C:24]2[C:19](=[CH:20][CH:21]=[CH:22][CH:23]=2)[N:18]=1>>[N:18]1[C:19]2[C:24](=[CH:23][CH:22]=[CH:21][CH:20]=2)[N:25]=[CH:26][C:17]=1[NH:15][CH2:14][CH:9]1[CH2:10][CH2:11][CH2:12][CH2:13][N:8]1[C:6]([OH:5])=[O:7]

Participants

3

Reactant 2

HCID 2389382-ChloroquinoxalineHCID 2756482tert-Butyl 2-(aminomethyl)piperidine-1-carboxylate

Product 1

HCID 67090637HCID 67090637, compound

Procedure

The title compound (0.73 g) was prepared from (RS) 2-aminomethyl-piperidine-1-carboxylic acid tert butyl ester (1 ml) and 2-chloroquinoxaline (0.5 g) according to the procedure of D8.

Sources & evidence

ORD record
ord-b66179b931514d56930b3a3b112bb50c
Source dataset
uspto-grants-2008_10
Patent number
US07432270B2

Reaction notes

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