Tert-butyl 3-formylazetidine-1-carboxylate → HCID 178425790, compound

HRID 1488060Notes

Reaction equation

HRID 1488060 reaction equation
[C:1]([C:3]1[CH:8]=[CH:7][C:6]([CH:9]2[CH2:12][N:11]([C:13]([C:15]3[CH:16]=[CH:17][C:18]([CH3:40])=[C:19]([C:21]4[N:22]=[C:23](C5CCN(C(OC(C)(C)C)=O)CC5)[NH:24][C:25]=4[CH3:26])[CH:20]=3)=[O:14])[CH2:10]2)=[CH:5][CH:4]=1)#[N:2].C([CH:43]1[CH2:46][N:45]([C:47]([O:49][C:50]([CH3:53])([CH3:52])[CH3:51])=[O:48])[CH2:44]1)=O>>[C:1]([C:3]1[CH:4]=[CH:5][C:6]([CH:9]2[CH2:12][N:11]([C:13]([C:15]3[CH:16]=[CH:17][C:18]([CH3:40])=[C:19]([C:21]4[NH:22][C:23]([CH:43]5[CH2:44][N:45]([C:47]([O:49][C:50]([CH3:53])([CH3:52])[CH3:51])=[O:48])[CH2:46]5)=[N:24][C:25]=4[CH3:26])[CH:20]=3)=[O:14])[CH2:10]2)=[CH:7][CH:8]=1)#[N:2]

Participants

3

Reactant 2

HCID 10726182Tert-butyl 3-formylazetidine-1-carboxylateHCID 90021783t-Butyl 4-(4-(5-(3-(4-cyanophenyl)azetidine-1-carbonyl)-2-methylphenyl)-5-methyl-1H-imidazol-2-yl)piperidine-1-carboxylate

Product 1

HCID 178425790HCID 178425790, compound

Procedure

The title compound was prepared using standard chemical manipulations and procedures similar to those used for the preparation of compound 182.3, except tert-butyl 3-formylazetidine-1-carboxylate was used in place of tert-butyl 4-formylpiperidine-1-carboxylate.

Sources & evidence

ORD record
ord-3d11494b9cea45f8b70df2aee38f7a2f
Source dataset
uspto-grants-2016_08
Patent number
US09428502B2

Reaction notes

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