ethyl 4-((1R,3S)-3-hydroxycyclohexylamino)-2-(methylthio)pyrimidine-5-carboxylate

Base Information

Chemical Name:ethyl 4-((1R,3S)-3-hydroxycyclohexylamino)-2-(methylthio)pyrimidine-5-carboxylate
CAS No.:1403864-02-7
Molecular Formula:C₁₄H₂₁N₃O₃S
Molecular Weight:311.405
Hs Code.:

Synonyms:ethyl 4-((1R,3S)-3-hydroxycyclohexylamino)-2-(methylthio)pyrimidine-5-carboxylate

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Chemical Property of ethyl 4-((1R,3S)-3-hydroxycyclohexylamino)-2-(methylthio)pyrimidine-5-carboxylate

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Technology Process of ethyl 4-((1R,3S)-3-hydroxycyclohexylamino)-2-(methylthio)pyrimidine-5-carboxylate

There total 6 articles about ethyl 4-((1R,3S)-3-hydroxycyclohexylamino)-2-(methylthio)pyrimidine-5-carboxylate 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: 85.0%

: 5909-24-0
4-chloro-2-methanesulfanylpyrimidine-5-carboxylic acid ethyl ester

: 1110772-04-7
(1S,3R)-3-aminocyclohexan-1-ol

: 1403864-02-7
ethyl 4-((1R,3S)-3-hydroxycyclohexylamino)-2-(methylthio)pyrimidine-5-carboxylate

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In ethanol; at 60 ℃; for 2h;

Reference yield:

: 1521-51-3,113667-32-6
rac-3-bromocyclohexene

: 1403864-02-7
ethyl 4-((1R,3S)-3-hydroxycyclohexylamino)-2-(methylthio)pyrimidine-5-carboxylate

Guidance literature:: Multi-step reaction with 6 steps

1.1: N,N-dimethyl-formamide / 30 h / 20 °C

2.1: N-Bromosuccinimide / ethanol; chloroform / 16 h / 20 °C

2.2: 2 h / 20 °C

3.1: methanol; tri-n-butyl-tin hydride / 2,2'-azobis(isobutyronitrile) / toluene / 64 h / 80 °C

4.1: Lipase B / tetrahydrofuran / 20 °C / Inert atmosphere

4.2: 20 °C

5.1: hydrazine / ethanol / 3 h / 100 °C

6.1: N-ethyl-N,N-diisopropylamine / ethanol / 2 h / 60 °C

With methanol; N-Bromosuccinimide; tri-n-butyl-tin hydride; N-ethyl-N,N-diisopropylamine; hydrazine; 2,2'-azobis(isobutyronitrile); In tetrahydrofuran; ethanol; chloroform; N,N-dimethyl-formamide; toluene;

Reference yield:

: 1541-26-0
2-cyclohex-2-enyl-isoindole-1,3-dione

: 1403864-02-7
ethyl 4-((1R,3S)-3-hydroxycyclohexylamino)-2-(methylthio)pyrimidine-5-carboxylate

Guidance literature:: Multi-step reaction with 5 steps

1.1: N-Bromosuccinimide / ethanol; chloroform / 16 h / 20 °C

1.2: 2 h / 20 °C

2.1: methanol; tri-n-butyl-tin hydride / 2,2'-azobis(isobutyronitrile) / toluene / 64 h / 80 °C

3.1: Lipase B / tetrahydrofuran / 20 °C / Inert atmosphere

3.2: 20 °C

4.1: hydrazine / ethanol / 3 h / 100 °C

5.1: N-ethyl-N,N-diisopropylamine / ethanol / 2 h / 60 °C

With methanol; N-Bromosuccinimide; tri-n-butyl-tin hydride; N-ethyl-N,N-diisopropylamine; hydrazine; 2,2'-azobis(isobutyronitrile); In tetrahydrofuran; ethanol; chloroform; toluene;