(2S)-benzenesulfonylamino-3-[4-{4-(pyrimidin-2-ylamino)piperidin-1-yl}benzoylamino]propionic acid

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Chemical Name:(2S)-benzenesulfonylamino-3-[4-{4-(pyrimidin-2-ylamino)piperidin-1-yl}benzoylamino]propionic acid
CAS No.:247033-64-3
Molecular Formula:C₂₅H₂₈N₆O₅S
Molecular Weight:524.601
Hs Code.:

Synonyms:(2S)-benzenesulfonylamino-3-[4-{4-(pyrimidin-2-ylamino)piperidin-1-yl}benzoylamino]propionic acid

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Chemical Property of (2S)-benzenesulfonylamino-3-[4-{4-(pyrimidin-2-ylamino)piperidin-1-yl}benzoylamino]propionic acid

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Technology Process of (2S)-benzenesulfonylamino-3-[4-{4-(pyrimidin-2-ylamino)piperidin-1-yl}benzoylamino]propionic acid

There total 9 articles about (2S)-benzenesulfonylamino-3-[4-{4-(pyrimidin-2-ylamino)piperidin-1-yl}benzoylamino]propionic acid 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: 100.0%

: 247033-63-2
tert-butyl (2S)-benzenesulfonylamino-3-[4-{4-(pyrimidin-2-ylamino)piperidin-1-yl}benzoylamino]propionate

: 247033-64-3
(2S)-benzenesulfonylamino-3-[4-{4-(pyrimidin-2-ylamino)piperidin-1-yl}benzoylamino]propionic acid

Guidance literature:: With trifluoroacetic acid; In dichloromethane; at 20 ℃; for 2h;
DOI:10.1016/j.bmc.2005.10.060

Reference yield:

: 5382-16-1
4-HYDROXYPIPERIDINE

: 247033-64-3
(2S)-benzenesulfonylamino-3-[4-{4-(pyrimidin-2-ylamino)piperidin-1-yl}benzoylamino]propionic acid

Guidance literature:: Multi-step reaction with 7 steps

1.1: 77 percent / dimethylsulfoxide / 72 h / 120 °C

2.1: 51 percent / P(n-Bu)3; 1,1'-(azodicarbonyl)dipiperidine / benzene / 23 h / 0 - 20 °C

3.1: 99 percent / hydrazine monohydrate / methanol / 16 h / 20 °C

4.1: 64 percent / (i-Pr)2NEt / dimethylformamide / 10 h / 125 °C

5.1: 82 percent / NaOH / methanol; tetrahydrofuran; H₂O / 8 h / 40 °C

6.1: (i-Pr)2NEt; BOP / dimethylformamide; CH₂Cl₂ / 3 h / 20 °C

6.2: 60 percent / (i-Pr)2NEt / dimethylformamide; CH₂Cl₂ / 2 h / -10 °C

7.1: 99 percent / CF₃CO₂H / CH₂Cl₂ / 2 h / 20 °C

With sodium hydroxide; tributylphosphine; (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; hydrazine hydrate; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; 1,1'-azodicarbonyl-dipiperidine; In tetrahydrofuran; methanol; dichloromethane; water; dimethyl sulfoxide; N,N-dimethyl-formamide; benzene;
DOI:10.1016/j.bmc.2005.10.061

Reference yield:

: 247034-90-8
4-{4-(Pyrimidin-2-ylamino)piperidin-1-yl}benzoic acid

: 247033-64-3
(2S)-benzenesulfonylamino-3-[4-{4-(pyrimidin-2-ylamino)piperidin-1-yl}benzoylamino]propionic acid

Guidance literature:: Multi-step reaction with 2 steps

1.1: (i-Pr)2NEt; BOP / dimethylformamide; CH₂Cl₂ / 3 h / 20 °C

1.2: 60 percent / (i-Pr)2NEt / dimethylformamide; CH₂Cl₂ / 2 h / -10 °C

2.1: 99 percent / CF₃CO₂H / CH₂Cl₂ / 2 h / 20 °C

With (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/j.bmc.2005.10.061