Azidomethyl 2,2-dimethylpropanoate → (5-((2-Methylpyridin-3-yloxy)methyl)-1H-1,2,3-triazol-1-yl)methyl pivalate

HRID 80662Notes

Reaction equation

HRID 80662 reaction equation
[CH3:1][C:2]1[C:7]([O:8][CH2:9][C:10]#[CH:11])=[CH:6][CH:5]=[CH:4][N:3]=1.[C:12]([O:18][CH2:19][N:20]=[N+:21]=[N-:22])(=[O:17])[C:13]([CH3:16])([CH3:15])[CH3:14].N1NN=C(COC2C=CC(N3C=NN=N3)=NC=2)C=1>>[C:12]([O:18][CH2:19][N:20]1[C:10]([CH2:9][O:8][C:7]2[C:2]([CH3:1])=[N:3][CH:4]=[CH:5][CH:6]=2)=[CH:11][N:22]=[N:21]1)(=[O:17])[C:13]([CH3:16])([CH3:15])[CH3:14]

Participants

4

Reactant 3

HCID 11521126Azidomethyl 2,2-dimethylpropanoateHCID 534409482-Methyl-3-[(prop-2-yn-1-yl)oxy]pyridineHCID 577083825-((2H-1,2,3-Triazol-4-yl)methoxy)-2-(1H-tetrazol-1-yl)pyridine

Product 1

HCID 57708380(5-((2-Methylpyridin-3-yloxy)methyl)-1H-1,2,3-triazol-1-yl)methyl pivalate

Procedure

The title compound was synthesized using 2-methyl-3-(prop-2-ynyloxy)pyridine and azidomethyl pivalate in a manner similar as that described in Intermediate 13, Step 3.

Sources & evidence

ORD record
ord-0f90406051104b23876669b5eadb5fab
Source dataset
uspto-grants-2014_09
Patent number
US08846675B2

Reaction notes

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