2-<1-(R)-(N-carbobenzyloxy-N-methylamino)-2(R)-phenyl-2-<4'-(1b-hydroxyethyl)phenoxy>ethyl>-4-benzyl-5-<(tert-butoxycarbonyl)amino>oxazole

Base Information

Chemical Name:2-<1-(R)-(N-carbobenzyloxy-N-methylamino)-2(R)-phenyl-2-<4'-(1b-hydroxyethyl)phenoxy>ethyl>-4-benzyl-5-<(tert-butoxycarbonyl)amino>oxazole
CAS No.:127086-89-9
Molecular Formula:C₄₀H₄₃N₃O₇
Molecular Weight:677.797
Hs Code.:

Synonyms:2-<1-(R)-(N-carbobenzyloxy-N-methylamino)-2(R)-phenyl-2-<4'-(1b-hydroxyethyl)phenoxy>ethyl>-4-benzyl-5-<(tert-butoxycarbonyl)amino>oxazole

Suppliers and Price of 2-<1-(R)-(N-carbobenzyloxy-N-methylamino)-2(R)-phenyl-2-<4'-(1b-hydroxyethyl)phenoxy>ethyl>-4-benzyl-5-<(tert-butoxycarbonyl)amino>oxazole

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 2-<1-(R)-(N-carbobenzyloxy-N-methylamino)-2(R)-phenyl-2-<4'-(1b-hydroxyethyl)phenoxy>ethyl>-4-benzyl-5-<(tert-butoxycarbonyl)amino>oxazole

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 2-<1-(R)-(N-carbobenzyloxy-N-methylamino)-2(R)-phenyl-2-<4'-(1b-hydroxyethyl)phenoxy>ethyl>-4-benzyl-5-<(tert-butoxycarbonyl)amino>oxazole

There total 15 articles about 2-<1-(R)-(N-carbobenzyloxy-N-methylamino)-2(R)-phenyl-2-<4'-(1b-hydroxyethyl)phenoxy>ethyl>-4-benzyl-5-<(tert-butoxycarbonyl)amino>oxazole 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: 89.0%

: 127086-88-8
2-<1-(R)-(N-carbobenzyloxy-N-methylamino)-2(R)-phenyl-2-<4-<(isopropoxycarbonyl)methyl>phenoxy>ethyl>-4-benzyl-5-<(tert-butoxycarbonyl)amino>oxazole

: 127086-89-9
2-<1-(R)-(N-carbobenzyloxy-N-methylamino)-2(R)-phenyl-2-<4'-(1b-hydroxyethyl)phenoxy>ethyl>-4-benzyl-5-<(tert-butoxycarbonyl)amino>oxazole

Guidance literature:: With lithium aluminium tetrahydride; In tetrahydrofuran; at 0 ℃; for 0.25h;
DOI:10.1021/ja00175a039

Reference yield:

: 156-38-7
4-hydroxyphenylacetate

: 127086-89-9
2-<1-(R)-(N-carbobenzyloxy-N-methylamino)-2(R)-phenyl-2-<4'-(1b-hydroxyethyl)phenoxy>ethyl>-4-benzyl-5-<(tert-butoxycarbonyl)amino>oxazole

Guidance literature:: Multi-step reaction with 8 steps

1: 97 percent / conc. H₂SO₄ / Heating

2: 90 percent / diethylazodicarboxylate, PPh₃ / tetrahydrofuran / Ambient temperature

3: 99 percent / trifluoracetic acid / CH₂Cl₂ / Ambient temperature

4: 3.63 g / NaIO₄, RuCl₃ dihydrate / acetonitrile; CCl₄; H₂O / 2 h / 0 °C

5: 1.) isobutyl chloroformate, N-methylmorpholine / 1.) THF, 0 deg C, 2.) 0 deg C, 4 h

6: 93 percent / trifluoroacetic acid / CH₂Cl₂ / 0 - 20 °C

7: 81 percent / DMAP, N-methylmorpholine / tetrahydrofuran / Ambient temperature

8: 89 percent / LiAlH₄ / tetrahydrofuran / 0.25 h / 0 °C

With 4-methyl-morpholine; dmap; ruthenium trichloride; sodium periodate; lithium aluminium tetrahydride; sulfuric acid; triphenylphosphine; trifluoroacetic acid; diethylazodicarboxylate; isobutyl chloroformate; In tetrahydrofuran; tetrachloromethane; dichloromethane; water; acetonitrile;
DOI:10.1021/ja00175a039

Reference yield:

: 34619-03-9
tert-butyldicarbonate

: 127086-89-9
2-<1-(R)-(N-carbobenzyloxy-N-methylamino)-2(R)-phenyl-2-<4'-(1b-hydroxyethyl)phenoxy>ethyl>-4-benzyl-5-<(tert-butoxycarbonyl)amino>oxazole

Guidance literature:: Multi-step reaction with 2 steps

1: 81 percent / DMAP, N-methylmorpholine / tetrahydrofuran / Ambient temperature

2: 89 percent / LiAlH₄ / tetrahydrofuran / 0.25 h / 0 °C

With 4-methyl-morpholine; dmap; lithium aluminium tetrahydride; In tetrahydrofuran;
DOI:10.1021/ja00175a039