2-Methylimidazole → HCID 66853367, compound

HRID 523105Notes

Reaction equation

HRID 523105 reaction equation
[CH3:1][C:2]1[NH:3][CH:4]=[CH:5][N:6]=1.S(O[CH2:18][CH:19]1[CH2:24][CH2:23][N:22]([C:25]([O:27][C:28]([CH3:31])([CH3:30])[CH3:29])=[O:26])[CH2:21][CH2:20]1)(C1C=CC(C)=CC=1)(=O)=O>>[CH3:1][C:2]1[N:3]([CH2:18][CH:19]2[CH2:24][CH2:23][N:22]([C:25]([O:27][C:28]([CH3:29])([CH3:31])[CH3:30])=[O:26])[CH2:21][CH2:20]2)[CH:4]=[CH:5][N:6]=1

Participants

3

Reactant 2

HCID 127492-MethylimidazoleHCID 106428511-(tert-Butoxycarbonyl)-4-((p-toluenesulfonyloxy)methyl)piperidine

Product 1

HCID 66853367HCID 66853367, compound

Procedure

The title compound was prepared according to the method described for Preparation 146 using 2-methyl-1H-imidazole and tert-butyl 4-((tosyloxy)methyl)piperidine-1-carboxylate.

Sources & evidence

ORD record
ord-bdb19c53deab45ea8381c5f36a74753e
Source dataset
uspto-grants-2016_05
Patent number
US09334286B2

Reaction notes

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