(S)-4-{(S)-3-[4-(Di-tert-butoxy-phosphoryloxy)-phenyl]-2-[3-(4-methoxy-phenyl)-ureido]-propionylamino}-4-dipentylcarbamoyl-butyric acid tert-butyl ester

Base Information

Chemical Name:(S)-4-{(S)-3-[4-(Di-tert-butoxy-phosphoryloxy)-phenyl]-2-[3-(4-methoxy-phenyl)-ureido]-propionylamino}-4-dipentylcarbamoyl-butyric acid tert-butyl ester
CAS No.:205236-62-0
Molecular Formula:C₄₄H₇₁N₄O₁₀P
Molecular Weight:847.042
Hs Code.:

(S)-4-{(S)-3-[4-(Di-tert-butoxy-phosphoryloxy)-phenyl]-2-[3-(4-methoxy-phenyl)-ureido]-propionylamino}-4-dipentylcarbamoyl-butyric acid tert-butyl ester

Synonyms:(S)-4-{(S)-3-[4-(Di-tert-butoxy-phosphoryloxy)-phenyl]-2-[3-(4-methoxy-phenyl)-ureido]-propionylamino}-4-dipentylcarbamoyl-butyric acid tert-butyl ester

Suppliers and Price of (S)-4-{(S)-3-[4-(Di-tert-butoxy-phosphoryloxy)-phenyl]-2-[3-(4-methoxy-phenyl)-ureido]-propionylamino}-4-dipentylcarbamoyl-butyric acid tert-butyl ester

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 (S)-4-{(S)-3-[4-(Di-tert-butoxy-phosphoryloxy)-phenyl]-2-[3-(4-methoxy-phenyl)-ureido]-propionylamino}-4-dipentylcarbamoyl-butyric acid tert-butyl ester

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (S)-4-{(S)-3-[4-(Di-tert-butoxy-phosphoryloxy)-phenyl]-2-[3-(4-methoxy-phenyl)-ureido]-propionylamino}-4-dipentylcarbamoyl-butyric acid tert-butyl ester

There total 7 articles about (S)-4-{(S)-3-[4-(Di-tert-butoxy-phosphoryloxy)-phenyl]-2-[3-(4-methoxy-phenyl)-ureido]-propionylamino}-4-dipentylcarbamoyl-butyric acid tert-butyl ester 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: 34.0%

: 5416-93-3
4-Methoxyphenyl isocyanate

: 205236-46-0
(S)-4-{(S)-2-Amino-3-[4-(di-tert-butoxy-phosphoryloxy)-phenyl]-propionylamino}-4-dipentylcarbamoyl-butyric acid tert-butyl ester

: 205236-62-0
(S)-4-{(S)-3-[4-(Di-tert-butoxy-phosphoryloxy)-phenyl]-2-[3-(4-methoxy-phenyl)-ureido]-propionylamino}-4-dipentylcarbamoyl-butyric acid tert-butyl ester

Guidance literature:: With dmap; In dichloromethane; at 0 - 20 ℃;
DOI:10.1021/jm970853a

Reference yield:

: 3886-08-6
5-tert-butyl N-benzyloxycarbonyl-L-glutamate

: 205236-62-0
(S)-4-{(S)-3-[4-(Di-tert-butoxy-phosphoryloxy)-phenyl]-2-[3-(4-methoxy-phenyl)-ureido]-propionylamino}-4-dipentylcarbamoyl-butyric acid tert-butyl ester

Guidance literature:: Multi-step reaction with 7 steps

1: 4-methylmorpholine / tetrahydrofuran / 0.08 h / -20 °C

2: tetrahydrofuran / 14 h / -20 - 20 °C

3: 90 percent / H₂ / 10percent Pd/C / methanol / 4 h / 760 Torr

4: 78 percent / DCC, HOBT, Et₃N / CH₂Cl₂; dimethylformamide / 16 h / 0 - 20 °C

5: 1.) NaH / 1.) THF, 0 deg C, 30 min, 2.) THF, from 0 deg C to RT, 4 h

6: 98 percent / H₂ / 10percent Pd/C / methanol / 3 h / 760 Torr

7: 34 percent / DMAP / CH₂Cl₂ / 0 - 20 °C

With 4-methyl-morpholine; dmap; hydrogen; sodium hydride; benzotriazol-1-ol; triethylamine; dicyclohexyl-carbodiimide; palladium on activated charcoal; In tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jm970853a

Reference yield:

: 41445-50-5
(S)-4-Benzyloxycarbonylamino-5-isobutoxycarbonyloxy-5-oxo-pentanoic acid tert-butyl ester

: 205236-62-0
(S)-4-{(S)-3-[4-(Di-tert-butoxy-phosphoryloxy)-phenyl]-2-[3-(4-methoxy-phenyl)-ureido]-propionylamino}-4-dipentylcarbamoyl-butyric acid tert-butyl ester

Guidance literature:: Multi-step reaction with 6 steps

1: tetrahydrofuran / 14 h / -20 - 20 °C

2: 90 percent / H₂ / 10percent Pd/C / methanol / 4 h / 760 Torr

3: 78 percent / DCC, HOBT, Et₃N / CH₂Cl₂; dimethylformamide / 16 h / 0 - 20 °C

4: 1.) NaH / 1.) THF, 0 deg C, 30 min, 2.) THF, from 0 deg C to RT, 4 h

5: 98 percent / H₂ / 10percent Pd/C / methanol / 3 h / 760 Torr

6: 34 percent / DMAP / CH₂Cl₂ / 0 - 20 °C

With dmap; hydrogen; sodium hydride; benzotriazol-1-ol; triethylamine; dicyclohexyl-carbodiimide; palladium on activated charcoal; In tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jm970853a