Pentanoic acid 8-benzyloxy-2-methyl-imidazo[1,2-a]pyridin-3-ylmethyl ester

Base Information

Chemical Name:Pentanoic acid 8-benzyloxy-2-methyl-imidazo[1,2-a]pyridin-3-ylmethyl ester
CAS No.:96428-69-2
Molecular Formula:C₂₁H₂₄N₂O₃
Molecular Weight:352.433
Hs Code.:

Synonyms:Pentanoic acid 8-benzyloxy-2-methyl-imidazo[1,2-a]pyridin-3-ylmethyl ester

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Chemical Property of Pentanoic acid 8-benzyloxy-2-methyl-imidazo[1,2-a]pyridin-3-ylmethyl ester

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Technology Process of Pentanoic acid 8-benzyloxy-2-methyl-imidazo[1,2-a]pyridin-3-ylmethyl ester

There total 3 articles about Pentanoic acid 8-benzyloxy-2-methyl-imidazo[1,2-a]pyridin-3-ylmethyl ester which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 88.0%

: 638-29-9
n-valeryl chloride

: 79707-34-9
3-(hydroxymethyl)-2-methyl-8-(phenylmethoxy)imidazo<1,2-a>pyridine

: 96428-69-2
Pentanoic acid 8-benzyloxy-2-methyl-imidazo[1,2-a]pyridin-3-ylmethyl ester

Guidance literature:: With triethylamine; In dichloromethane; for 3h;
DOI:10.1021/jm00145a006

Reference yield:

: 24016-03-3
2-amino-3-benzyloxypyridine

: 96428-69-2
Pentanoic acid 8-benzyloxy-2-methyl-imidazo[1,2-a]pyridin-3-ylmethyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 28 percent / ethanol / 20 h / Heating

2: 65 percent / lithium aluminum hydride / tetrahydrofuran / 1 h / 0 - 5 °C

3: 88 percent / triethylamine / CH₂Cl₂ / 3 h

With lithium aluminium tetrahydride; triethylamine; In tetrahydrofuran; ethanol; dichloromethane;
DOI:10.1021/jm00145a006

Reference yield:

: 96428-50-1
2-carboethoxy-3-methyl-8-(phenylmethoxy)imidazo<1,2-a>pyridine

: 96428-69-2
Pentanoic acid 8-benzyloxy-2-methyl-imidazo[1,2-a]pyridin-3-ylmethyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 65 percent / lithium aluminum hydride / tetrahydrofuran / 1 h / 0 - 5 °C

2: 88 percent / triethylamine / CH₂Cl₂ / 3 h

With lithium aluminium tetrahydride; triethylamine; In tetrahydrofuran; dichloromethane;
DOI:10.1021/jm00145a006