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3-Pyridinecarboxylic acid, 6-(acetylamino)-1-(2-ethyl-1-oxobutyl)-1,2,5,6-tetrahydro-5-hydroxy-, diphenylmethyl ester, (5S,6S)-

Base Information
  • Chemical Name:3-Pyridinecarboxylic acid, 6-(acetylamino)-1-(2-ethyl-1-oxobutyl)-1,2,5,6-tetrahydro-5-hydroxy-, diphenylmethyl ester, (5S,6S)-
  • CAS No.:315700-24-4
  • Molecular Formula:C27H32N2O5
  • Molecular Weight:464.561
  • Hs Code.:
3-Pyridinecarboxylic acid,
6-(acetylamino)-1-(2-ethyl-1-oxobutyl)-1,2,5,6-tetrahydro-5-hydroxy-,
diphenylmethyl ester, (5S,6S)-

Synonyms:

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Chemical Property of 3-Pyridinecarboxylic acid, 6-(acetylamino)-1-(2-ethyl-1-oxobutyl)-1,2,5,6-tetrahydro-5-hydroxy-, diphenylmethyl ester, (5S,6S)-
Chemical Property:
Purity/Quality:
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Technology Process of 3-Pyridinecarboxylic acid, 6-(acetylamino)-1-(2-ethyl-1-oxobutyl)-1,2,5,6-tetrahydro-5-hydroxy-, diphenylmethyl ester, (5S,6S)-

There total 4 articles about 3-Pyridinecarboxylic acid, 6-(acetylamino)-1-(2-ethyl-1-oxobutyl)-1,2,5,6-tetrahydro-5-hydroxy-, diphenylmethyl ester, (5S,6S)- 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:
Guidance literature:
Multi-step reaction with 4 steps
1: pyridine / 20 °C
2: 1,8-diazabicyclo[5.4.0]undec-7-ene / benzene
3: sodium hydroxide / methanol; water / 20 °C
4: methanol / 20 °C
With pyridine; sodium hydroxide; 1,8-diazabicyclo[5.4.0]undec-7-ene; In methanol; water; benzene; 1: Acylation / 2: Dehydration / 3: Hydrolysis / 4: Alkylation;
DOI:10.1021/ol000261d
Guidance literature:
Multi-step reaction with 2 steps
1: sodium hydroxide / methanol; water / 20 °C
2: methanol / 20 °C
With sodium hydroxide; In methanol; water; 1: Hydrolysis / 2: Alkylation;
DOI:10.1021/ol000261d
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