4-Amino-2,2,6,6-tetramethylpiperidine → HCID 178440488, compound

HRID 46088

Reaction equation

HRID 46088 reaction equation
[NH2:1][C:2]1[O:3][CH:4]([CH:8]([CH3:10])[CH3:9])[C:5](=[O:7])[N:6]=1.N[CH:12]1[CH2:17][C:16]([CH3:19])([CH3:18])[NH:15][C:14]([CH3:21])([CH3:20])[CH2:13]1>>[CH:8]([CH:4]1[O:3][C:2]([NH:1][CH:12]2[CH2:17][C:16]([CH3:19])([CH3:18])[NH:15][C:14]([CH3:21])([CH3:20])[CH2:13]2)=[N:6][C:5]1=[O:7])([CH3:10])[CH3:9]

Participants

3

Reactant 2

HCID 375244-Amino-2,2,6,6-tetramethylpiperidineHCID 49617292-amino-5-isopropyl-1,3-oxazol-4(5H)-one

Product 1

HCID 178440488HCID 178440488, compound

Procedure

Synthesis was performed from 2-amino-5-isopropyl-1,3-oxazol-4(5H)-one and 4-amino-2,2,6,6-tetramethylpiperidine according to Method G+H.

Workup

  1. customSynthesis

Sources & evidence

ORD record
ord-1156fcba1ba34b2aae01911adc162f39
Source dataset
uspto-grants-2013_09
Patent number
US08541592B2

Linked notes

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