(S)-3-[3-(6-Benzyloxycarbonylamino-hexanoylamino)-4-methoxy-phenyl]-2-(3-trifluoromethyl-benzenesulfonylamino)-propionic acid tert-butyl ester

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Chemical Name:(S)-3-[3-(6-Benzyloxycarbonylamino-hexanoylamino)-4-methoxy-phenyl]-2-(3-trifluoromethyl-benzenesulfonylamino)-propionic acid tert-butyl ester
CAS No.:216502-88-4
Molecular Formula:C₃₅H₄₂F₃N₃O₈S
Molecular Weight:721.795
Hs Code.:

(S)-3-[3-(6-Benzyloxycarbonylamino-hexanoylamino)-4-methoxy-phenyl]-2-(3-trifluoromethyl-benzenesulfonylamino)-propionic acid tert-butyl ester

Synonyms:(S)-3-[3-(6-Benzyloxycarbonylamino-hexanoylamino)-4-methoxy-phenyl]-2-(3-trifluoromethyl-benzenesulfonylamino)-propionic acid tert-butyl ester

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Chemical Property of (S)-3-[3-(6-Benzyloxycarbonylamino-hexanoylamino)-4-methoxy-phenyl]-2-(3-trifluoromethyl-benzenesulfonylamino)-propionic acid tert-butyl ester

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Technology Process of (S)-3-[3-(6-Benzyloxycarbonylamino-hexanoylamino)-4-methoxy-phenyl]-2-(3-trifluoromethyl-benzenesulfonylamino)-propionic acid tert-butyl ester

There total 8 articles about (S)-3-[3-(6-Benzyloxycarbonylamino-hexanoylamino)-4-methoxy-phenyl]-2-(3-trifluoromethyl-benzenesulfonylamino)-propionic 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: 48.0%

: 4644-75-1
6-benzyloxycarbonylaminocapronoyl chloride

: 216502-87-3
t-butyl O-methyl-meta-amino-N-[3-(trifluoromethyl)phenylsulfonyl]-L-tyrosinate

: 216502-88-4
(S)-3-[3-(6-Benzyloxycarbonylamino-hexanoylamino)-4-methoxy-phenyl]-2-(3-trifluoromethyl-benzenesulfonylamino)-propionic acid tert-butyl ester

Guidance literature:: With pyridine; In dichloromethane; at 20 ℃; for 20h;
DOI:10.1016/S0968-0896(98)00083-2

Reference yield:

: 777-44-6
3-(Trifluoromethyl)benzenesulfonyl chloride

: 216502-88-4
(S)-3-[3-(6-Benzyloxycarbonylamino-hexanoylamino)-4-methoxy-phenyl]-2-(3-trifluoromethyl-benzenesulfonylamino)-propionic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 51 percent / Et₃N / CH₂Cl₂ / 20 h / 20 °C

2: 91 percent / H₂ / PtO₂ / methanol / 17 h / 20 °C / 2068.6 Torr

3: 48 percent / pyridine / CH₂Cl₂ / 20 h / 20 °C

With pyridine; hydrogen; triethylamine; platinum(IV) oxide; In methanol; dichloromethane;
DOI:10.1016/S0968-0896(98)00083-2

Reference yield:

: 16874-12-7,87553-74-0
Tyr(tBu)

: 216502-88-4
(S)-3-[3-(6-Benzyloxycarbonylamino-hexanoylamino)-4-methoxy-phenyl]-2-(3-trifluoromethyl-benzenesulfonylamino)-propionic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 6 steps

1: 2.) conc. HNO₃, AcOH / 1.) room temperature, 30 min, 2.) 10-14 deg C, 75 min

2: 72 percent / K₂CO₃, <18-c-6>crown-ether / acetonitrile / 48 h / Heating

3: 88 percent / K₂CO₃ / methanol; H₂O / 17 h / 20 °C

4: 51 percent / Et₃N / CH₂Cl₂ / 20 h / 20 °C

5: 91 percent / H₂ / PtO₂ / methanol / 17 h / 20 °C / 2068.6 Torr

6: 48 percent / pyridine / CH₂Cl₂ / 20 h / 20 °C

With pyridine; 18-crown-6 ether; hydrogen; nitric acid; potassium carbonate; acetic acid; triethylamine; platinum(IV) oxide; In methanol; dichloromethane; water; acetonitrile;
DOI:10.1016/S0968-0896(98)00083-2