{(S)-1-[(4R,5R)-5-((S)-1-tert-Butoxycarbonylamino-2-phenoxy-ethyl)-2-thioxo-[1,3]dioxolan-4-yl]-2-phenoxy-ethyl}-carbamic acid tert-butyl ester

Base Information

Chemical Name:{(S)-1-[(4R,5R)-5-((S)-1-tert-Butoxycarbonylamino-2-phenoxy-ethyl)-2-thioxo-[1,3]dioxolan-4-yl]-2-phenoxy-ethyl}-carbamic acid tert-butyl ester
CAS No.:211994-14-8
Molecular Formula:C₂₉H₃₈N₂O₈S
Molecular Weight:574.695
Hs Code.:

Synonyms:{(S)-1-[(4R,5R)-5-((S)-1-tert-Butoxycarbonylamino-2-phenoxy-ethyl)-2-thioxo-[1,3]dioxolan-4-yl]-2-phenoxy-ethyl}-carbamic acid tert-butyl ester

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Chemical Property of {(S)-1-[(4R,5R)-5-((S)-1-tert-Butoxycarbonylamino-2-phenoxy-ethyl)-2-thioxo-[1,3]dioxolan-4-yl]-2-phenoxy-ethyl}-carbamic acid tert-butyl ester

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Technology Process of {(S)-1-[(4R,5R)-5-((S)-1-tert-Butoxycarbonylamino-2-phenoxy-ethyl)-2-thioxo-[1,3]dioxolan-4-yl]-2-phenoxy-ethyl}-carbamic acid tert-butyl ester

There total 10 articles about {(S)-1-[(4R,5R)-5-((S)-1-tert-Butoxycarbonylamino-2-phenoxy-ethyl)-2-thioxo-[1,3]dioxolan-4-yl]-2-phenoxy-ethyl}-carbamic 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: 70.0%

: 6160-65-2
1,1'-Thiocarbonyldiimidazole

: 211993-86-1
((1S,2R,3R,4S)-4-tert-Butoxycarbonylamino-2,3-dihydroxy-5-phenoxy-1-phenoxymethyl-pentyl)-carbamic acid tert-butyl ester

: {(S)-1-[(4R,5R)-5-((S)-1-tert-Butoxycarbonylamino-2-phenoxy-ethyl)-2-oxo-[1,3]dioxolan-4-yl]-2-phenoxy-ethyl}-carbamic acid tert-butyl ester

: 211994-14-8
{(S)-1-[(4R,5R)-5-((S)-1-tert-Butoxycarbonylamino-2-phenoxy-ethyl)-2-thioxo-[1,3]dioxolan-4-yl]-2-phenoxy-ethyl}-carbamic acid tert-butyl ester

Guidance literature:: In tetrahydrofuran; at 55 ℃; for 22h;
DOI:10.1021/jo971562c

Reference yield:

: 24424-99-5
di-tert-butyl dicarbonate

: 211994-14-8
{(S)-1-[(4R,5R)-5-((S)-1-tert-Butoxycarbonylamino-2-phenoxy-ethyl)-2-thioxo-[1,3]dioxolan-4-yl]-2-phenoxy-ethyl}-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 92 percent / H₂ / Pd/C / ethyl acetate / 3 h

2: 70 percent / tetrahydrofuran / 22 h / 55 °C

With hydrogen; palladium on activated charcoal; In tetrahydrofuran; ethyl acetate;
DOI:10.1021/jo971562c

Reference yield:

: 211993-84-9
2,5-diazido-2,5-dideoxy-1,6-di-O-phenyl-L-iditol

: 211994-14-8
{(S)-1-[(4R,5R)-5-((S)-1-tert-Butoxycarbonylamino-2-phenoxy-ethyl)-2-thioxo-[1,3]dioxolan-4-yl]-2-phenoxy-ethyl}-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 6 steps

1: H₂ / Pd/C / ethyl acetate / 16 h

2: 28 percent / Et₃N / CH₂Cl₂ / Ambient temperature

3: 0.050 g / CrO₃, Ac₂O, pyridine / CH₂Cl₂ / 3 h

4: 1.) NaBH₄, 2.) Ba(OH)2*8H₂O / 1.) MeOH, 1 h, 2.) H₂O, 80 deg C, 24 h

5: ethyl acetate / 4 h

6: 70 percent / tetrahydrofuran / 22 h / 55 °C

With pyridine; chromium(VI) oxide; barium dihydroxide; sodium tetrahydroborate; hydrogen; acetic anhydride; triethylamine; palladium on activated charcoal; In tetrahydrofuran; dichloromethane; ethyl acetate;
DOI:10.1021/jo971562c