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3,6-dihydro-4-methyl-2-thioxo-6-<2-(trifluoromethyl)phenyl>-1,5(2H)-pyrimidinedicarboxylic acid 5-ethyl 1-<1-(phenylmethyl)-4-piperidinyl> diester monohydrochloride

Base Information
  • Chemical Name:3,6-dihydro-4-methyl-2-thioxo-6-<2-(trifluoromethyl)phenyl>-1,5(2H)-pyrimidinedicarboxylic acid 5-ethyl 1-<1-(phenylmethyl)-4-piperidinyl> diester monohydrochloride
  • CAS No.:108931-33-5
  • Molecular Formula:C28H30F3N3O4S*ClH
  • Molecular Weight:598.086
  • Hs Code.:
3,6-dihydro-4-methyl-2-thioxo-6-<2-(trifluoromethyl)phenyl>-1,5(2H)-pyrimidinedicarboxylic acid 5-ethyl 1-<1-(phenylmethyl)-4-piperidinyl> diester monohydrochloride

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Chemical Property of 3,6-dihydro-4-methyl-2-thioxo-6-<2-(trifluoromethyl)phenyl>-1,5(2H)-pyrimidinedicarboxylic acid 5-ethyl 1-<1-(phenylmethyl)-4-piperidinyl> diester monohydrochloride
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Technology Process of 3,6-dihydro-4-methyl-2-thioxo-6-<2-(trifluoromethyl)phenyl>-1,5(2H)-pyrimidinedicarboxylic acid 5-ethyl 1-<1-(phenylmethyl)-4-piperidinyl> diester monohydrochloride

There total 6 articles about 3,6-dihydro-4-methyl-2-thioxo-6-<2-(trifluoromethyl)phenyl>-1,5(2H)-pyrimidinedicarboxylic acid 5-ethyl 1-<1-(phenylmethyl)-4-piperidinyl> diester monohydrochloride 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: 64 percent / sodium acetate / dimethylformamide / 4 h / 70 °C
2: pyridine / acetonitrile; toluene / 6 h / Ambient temperature
3: 6.4 g / acetonitrile / 16 h / Ambient temperature
4: 3.7 g / trifluoroacetic acid, ethanethiol / CH2Cl2 / 6 h / Ambient temperature
With pyridine; sodium acetate; trifluoroacetic acid; ethanethiol; In dichloromethane; N,N-dimethyl-formamide; toluene; acetonitrile;
DOI:10.1021/jo00286a020
Guidance literature:
Multi-step reaction with 2 steps
1: 6.4 g / acetonitrile / 16 h / Ambient temperature
2: 3.7 g / trifluoroacetic acid, ethanethiol / CH2Cl2 / 6 h / Ambient temperature
With trifluoroacetic acid; ethanethiol; In dichloromethane; acetonitrile;
DOI:10.1021/jo00286a020
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