4-N-Boc-4-N-Methyl-aminopiperidine → HCID 58071488, compound

HRID 1255994Notes

Reaction equation

HRID 1255994 reaction equation
F[C:2]1[CH:7]=[CH:6][C:5]([N+:8]([O-:10])=[O:9])=[C:4]([O:11][CH3:12])[CH:3]=1.[CH3:13][N:14]([CH:22]1[CH2:27][CH2:26][NH:25][CH2:24][CH2:23]1)[C:15](=[O:21])[O:16][C:17]([CH3:20])([CH3:19])[CH3:18]>>[CH3:12][O:11][C:4]1[CH:3]=[C:2]([N:25]2[CH2:24][CH2:23][CH:22]([N:14]([CH3:13])[C:15](=[O:21])[O:16][C:17]([CH3:18])([CH3:19])[CH3:20])[CH2:27][CH2:26]2)[CH:7]=[CH:6][C:5]=1[N+:8]([O-:10])=[O:9]

Participants

3

Reactant 2

HCID 27568064-N-Boc-4-N-Methyl-aminopiperidineHCID 27792505-Fluoro-2-nitroanisole

Product 1

HCID 58071488HCID 58071488, compound

Procedure

Starting materials: 4-fluoro-2-methoxy-1-nitrobenzene and tert-butyl methyl(piperidin-4-yl)carbamate. m/z 366.

Sources & evidence

ORD record
ord-2b60a47aec1b4071866421e567f6a109
Source dataset
uspto-grants-2013_06
Patent number
US08461170B2

Reaction notes

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