Piperidine → HCID 22981345, compound

HRID 1861964Notes

Reaction equation

[C:1]([O:5][C:6]([N:8]([C:20]([O:22][C:23]([CH3:26])([CH3:25])[CH3:24])=[O:21])[CH2:9][C:10]1[CH:15]=[C:14]([N+:16]([O-:18])=[O:17])[CH:13]=[CH:12][C:11]=1F)=[O:7])([CH3:4])([CH3:3])[CH3:2].[NH:27]1[CH2:32][CH2:31][CH2:30][CH2:29][CH2:28]1>>[C:1]([O:5][C:6]([N:8]([C:20]([O:22][C:23]([CH3:26])([CH3:25])[CH3:24])=[O:21])[CH2:9][C:10]1[CH:15]=[C:14]([N+:16]([O-:18])=[O:17])[CH:13]=[CH:12][C:11]=1[N:27]1[CH2:32][CH2:31][CH2:30][CH2:29][CH2:28]1)=[O:7])([CH3:4])([CH3:3])[CH3:2]

Participants

Reactant 2

HCID 8082Piperidine

HCID 22981229HCID 22981229, compound

Product 1

HCID 22981345HCID 22981345, compoundYield 98%

Procedure

Using the compound obtained in Example 263 as a starting material and also using piperidine as a reagent in the absence of a solvent, the same procedure of Example 264 gave 1.524 g of the titled compound (yield, 98%).

Sources & evidence

ORD record: ord-762b02a11aec49a28e2b24d3ef10d6ea
Source dataset: uspto-grants-2003_03
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US06534546B1

Reaction notes

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