4-hydroxy-3-[(phenoxyacetyl)amino]-1-piperidinecarboxylic acid 1,1-dimethylethyl ester

Base Information

Chemical Name:4-hydroxy-3-[(phenoxyacetyl)amino]-1-piperidinecarboxylic acid 1,1-dimethylethyl ester
CAS No.:1363286-63-8
Molecular Formula:C₁₈H₂₆N₂O₅
Molecular Weight:350.415
Hs Code.:

Synonyms:4-hydroxy-3-[(phenoxyacetyl)amino]-1-piperidinecarboxylic acid 1,1-dimethylethyl ester

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Chemical Property of 4-hydroxy-3-[(phenoxyacetyl)amino]-1-piperidinecarboxylic acid 1,1-dimethylethyl ester

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Technology Process of 4-hydroxy-3-[(phenoxyacetyl)amino]-1-piperidinecarboxylic acid 1,1-dimethylethyl ester

There total 3 articles about 4-hydroxy-3-[(phenoxyacetyl)amino]-1-piperidinecarboxylic acid 1,1-dimethylethyl 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:

: 85838-94-4
N-Boc-1,2,3,6-tetrahydropyridine

: 1363286-63-8
4-hydroxy-3-[(phenoxyacetyl)amino]-1-piperidinecarboxylic acid 1,1-dimethylethyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 0 - 20 °C

2: sodium azide; ammonium chloride / ethanol; water / 0.08 h / 150 °C / microwave irradiation

3: hydrogen / palladium 10% on activated carbon / ethanol / 50 °C

4: triethylamine / dichloromethane / 0.25 h / 0 - 20 °C

With sodium azide; hydrogen; ammonium chloride; triethylamine; 3-chloro-benzenecarboperoxoic acid; palladium 10% on activated carbon; In ethanol; dichloromethane; water;

Reference yield:

: 161157-50-2
tert-butyl 7-oxa-3-azabicyclo[4.1.0]heptane-3-carboxylate

: 1363286-63-8
4-hydroxy-3-[(phenoxyacetyl)amino]-1-piperidinecarboxylic acid 1,1-dimethylethyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: sodium azide; ammonium chloride / ethanol; water / 0.08 h / 150 °C / microwave irradiation

2: hydrogen / palladium 10% on activated carbon / ethanol / 50 °C

3: triethylamine / dichloromethane / 0.25 h / 0 - 20 °C

With sodium azide; hydrogen; ammonium chloride; triethylamine; palladium 10% on activated carbon; In ethanol; dichloromethane; water;

Reference yield:

: tert-butyl 3-azido-4-hydroxypiperidine-1-carboxylate

: 1363286-63-8
4-hydroxy-3-[(phenoxyacetyl)amino]-1-piperidinecarboxylic acid 1,1-dimethylethyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: hydrogen / palladium 10% on activated carbon / ethanol / 50 °C

2: triethylamine / dichloromethane / 0.25 h / 0 - 20 °C

With hydrogen; triethylamine; palladium 10% on activated carbon; In ethanol; dichloromethane;