tert-butyl (2S)-benzenesulfonylamino-3-[4-{4-(4,5,6,7-tetrahydro-1H-[1,3]diazepin-2-ylamino)piperidin-1-yl}benzoylamino]propionate

Base Information

Chemical Name:tert-butyl (2S)-benzenesulfonylamino-3-[4-{4-(4,5,6,7-tetrahydro-1H-[1,3]diazepin-2-ylamino)piperidin-1-yl}benzoylamino]propionate
CAS No.:247034-04-4
Molecular Formula:C₃₀H₄₂N₆O₅S
Molecular Weight:598.767
Hs Code.:

Synonyms:tert-butyl (2S)-benzenesulfonylamino-3-[4-{4-(4,5,6,7-tetrahydro-1H-[1,3]diazepin-2-ylamino)piperidin-1-yl}benzoylamino]propionate

Suppliers and Price of tert-butyl (2S)-benzenesulfonylamino-3-[4-{4-(4,5,6,7-tetrahydro-1H-[1,3]diazepin-2-ylamino)piperidin-1-yl}benzoylamino]propionate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of tert-butyl (2S)-benzenesulfonylamino-3-[4-{4-(4,5,6,7-tetrahydro-1H-[1,3]diazepin-2-ylamino)piperidin-1-yl}benzoylamino]propionate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of tert-butyl (2S)-benzenesulfonylamino-3-[4-{4-(4,5,6,7-tetrahydro-1H-[1,3]diazepin-2-ylamino)piperidin-1-yl}benzoylamino]propionate

There total 9 articles about tert-butyl (2S)-benzenesulfonylamino-3-[4-{4-(4,5,6,7-tetrahydro-1H-[1,3]diazepin-2-ylamino)piperidin-1-yl}benzoylamino]propionate 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: 26.0%

: 883727-01-3
4-{4-(4,5,6,7-tetrahydro-1H-[1,3]diazepin-2-ylamino)piperidin-1-yl}benzoic acid

: tert-butyl (2S)-N-benzenesulfonyl-2,3-diaminopropionate hydrochloride

: 247034-04-4
tert-butyl (2S)-benzenesulfonylamino-3-[4-{4-(4,5,6,7-tetrahydro-1H-[1,3]diazepin-2-ylamino)piperidin-1-yl}benzoylamino]propionate

Guidance literature:: 4-{4-(4,5,6,7-tetrahydro-1H-[1,3]diazepin-2-ylamino)piperidin-1-yl}benzoic acid; With 1,1'-carbonyldiimidazole; In N,N-dimethyl-formamide; at 20 ℃; for 1.5h;

tert-butyl (2S)-N-benzenesulfonyl-2,3-diaminopropionate hydrochloride; In N,N-dimethyl-formamide; at 60 ℃; for 15h;
DOI:10.1016/j.bmc.2005.10.061

Reference yield:

: 247034-88-4
ethyl 4-(4-aminopiperidin-1-yl)benzoate

: 247034-04-4
tert-butyl (2S)-benzenesulfonylamino-3-[4-{4-(4,5,6,7-tetrahydro-1H-[1,3]diazepin-2-ylamino)piperidin-1-yl}benzoylamino]propionate

Guidance literature:: Multi-step reaction with 4 steps

1.1: tetrahydrofuran / 19 h / 20 °C

2.1: EtBr / ethanol / 13 h / Heating

2.2: CF₃CO₂H / H₂O / 3 h / 20 °C

2.3: NaOEt / ethanol / 16 h

3.1: 4.50 mg / NaOH / methanol; tetrahydrofuran; H₂O / 8 h / 40 °C

4.1: 1,1'-carbonyldiimidazole / dimethylformamide / 1.5 h / 20 °C

4.2: 26 percent / dimethylformamide / 15 h / 60 °C

With sodium hydroxide; ethidium Bromide; 1,1'-carbonyldiimidazole; In tetrahydrofuran; methanol; ethanol; water; N,N-dimethyl-formamide;
DOI:10.1016/j.bmc.2005.10.061

Reference yield:

: 5382-16-1
4-HYDROXYPIPERIDINE

: 247034-04-4
tert-butyl (2S)-benzenesulfonylamino-3-[4-{4-(4,5,6,7-tetrahydro-1H-[1,3]diazepin-2-ylamino)piperidin-1-yl}benzoylamino]propionate

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: tetrahydrofuran / 19 h / 20 °C

5.1: EtBr / ethanol / 13 h / Heating

5.2: CF₃CO₂H / H₂O / 3 h / 20 °C

5.3: NaOEt / ethanol / 16 h

6.1: 4.50 mg / NaOH / methanol; tetrahydrofuran; H₂O / 8 h / 40 °C

7.1: 1,1'-carbonyldiimidazole / dimethylformamide / 1.5 h / 20 °C

7.2: 26 percent / dimethylformamide / 15 h / 60 °C

With sodium hydroxide; tributylphosphine; ethidium Bromide; hydrazine hydrate; 1,1'-carbonyldiimidazole; 1,1'-azodicarbonyl-dipiperidine; In tetrahydrofuran; methanol; ethanol; water; dimethyl sulfoxide; N,N-dimethyl-formamide; benzene;
DOI:10.1016/j.bmc.2005.10.061