(S)-3-cyclohexyl-N-[1-((R)-2,3-dihydroxy-propyl)-1H-pyrazol-3-yl]-2-(8-methoxy-3-oxo-3,9-dihydro-1H-chromeno[2,3-c]pyrrol-2-yl)-propionamide

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Chemical Name:(S)-3-cyclohexyl-N-[1-((R)-2,3-dihydroxy-propyl)-1H-pyrazol-3-yl]-2-(8-methoxy-3-oxo-3,9-dihydro-1H-chromeno[2,3-c]pyrrol-2-yl)-propionamide
CAS No.:1352639-77-0
Molecular Formula:C₂₇H₃₄N₄O₆
Molecular Weight:510.59
Hs Code.:

Synonyms:(S)-3-cyclohexyl-N-[1-((R)-2,3-dihydroxy-propyl)-1H-pyrazol-3-yl]-2-(8-methoxy-3-oxo-3,9-dihydro-1H-chromeno[2,3-c]pyrrol-2-yl)-propionamide

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Chemical Property of (S)-3-cyclohexyl-N-[1-((R)-2,3-dihydroxy-propyl)-1H-pyrazol-3-yl]-2-(8-methoxy-3-oxo-3,9-dihydro-1H-chromeno[2,3-c]pyrrol-2-yl)-propionamide

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Technology Process of (S)-3-cyclohexyl-N-[1-((R)-2,3-dihydroxy-propyl)-1H-pyrazol-3-yl]-2-(8-methoxy-3-oxo-3,9-dihydro-1H-chromeno[2,3-c]pyrrol-2-yl)-propionamide

There total 5 articles about (S)-3-cyclohexyl-N-[1-((R)-2,3-dihydroxy-propyl)-1H-pyrazol-3-yl]-2-(8-methoxy-3-oxo-3,9-dihydro-1H-chromeno[2,3-c]pyrrol-2-yl)-propionamide 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: 52.7%

: 1352639-79-2
(S)-3-cyclohexyl-N-[1-((R)-2,2-dimethyl-[1,3]dioxolan-4-ylmethyl)-1H-pyrazol-3-yl]-2-(8-methoxy-3-oxo-3,9-dihydro-1H-chromeno[2,3-c]pyrrol-2-yl)-propionamide

: 1352639-77-0
(S)-3-cyclohexyl-N-[1-((R)-2,3-dihydroxy-propyl)-1H-pyrazol-3-yl]-2-(8-methoxy-3-oxo-3,9-dihydro-1H-chromeno[2,3-c]pyrrol-2-yl)-propionamide

Guidance literature:: With hydrogenchloride; water; In tetrahydrofuran; at 23 ℃; for 4h;

Reference yield:

: 700-44-7
6-methoxysalicylaldehyde

: 1352639-77-0
(S)-3-cyclohexyl-N-[1-((R)-2,3-dihydroxy-propyl)-1H-pyrazol-3-yl]-2-(8-methoxy-3-oxo-3,9-dihydro-1H-chromeno[2,3-c]pyrrol-2-yl)-propionamide

Guidance literature:: Multi-step reaction with 6 steps

1.1: pyrrolidine / dimethyl sulfoxide / 78 h / 25 °C

2.1: N-ethyl-N,N-diisopropylamine / methanol / 10 h / 25 °C / Molecular sieve

2.2: 16 h / 25 °C / Molecular sieve

3.1: N-ethyl-N,N-diisopropylamine / acetonitrile / 48 h / 140 °C / Sealed tube

4.1: water; lithium hydroxide monohydrate / tetrahydrofuran / 2 h / 25 °C

5.1: 4-methyl-morpholine; HATU / tetrahydrofuran / 24 h / 90 °C / Sealed tube

6.1: hydrogenchloride; water / tetrahydrofuran / 4 h / 23 °C

With pyrrolidine; 4-methyl-morpholine; hydrogenchloride; lithium hydroxide monohydrate; water; N-ethyl-N,N-diisopropylamine; HATU; In tetrahydrofuran; methanol; dimethyl sulfoxide; acetonitrile;

Reference yield:

: 40056-18-6,789460-77-1
methyl L-cyclohexylalaninate

: 1352639-77-0
(S)-3-cyclohexyl-N-[1-((R)-2,3-dihydroxy-propyl)-1H-pyrazol-3-yl]-2-(8-methoxy-3-oxo-3,9-dihydro-1H-chromeno[2,3-c]pyrrol-2-yl)-propionamide

Guidance literature:: Multi-step reaction with 5 steps

1.1: N-ethyl-N,N-diisopropylamine / methanol / 10 h / 25 °C / Molecular sieve

1.2: 16 h / 25 °C / Molecular sieve

2.1: N-ethyl-N,N-diisopropylamine / acetonitrile / 48 h / 140 °C / Sealed tube

3.1: water; lithium hydroxide monohydrate / tetrahydrofuran / 2 h / 25 °C

4.1: 4-methyl-morpholine; HATU / tetrahydrofuran / 24 h / 90 °C / Sealed tube

5.1: hydrogenchloride; water / tetrahydrofuran / 4 h / 23 °C

With 4-methyl-morpholine; hydrogenchloride; lithium hydroxide monohydrate; water; N-ethyl-N,N-diisopropylamine; HATU; In tetrahydrofuran; methanol; acetonitrile;