(S)-2-Benzyloxycarbonylamino-3-{3-[4-((S)-2-benzyloxycarbonyl-2-benzyloxycarbonylamino-ethyl)-phenoxy]-4-methoxy-phenyl}-propionic acid benzyl ester

Base Information

Chemical Name:(S)-2-Benzyloxycarbonylamino-3-{3-[4-((S)-2-benzyloxycarbonyl-2-benzyloxycarbonylamino-ethyl)-phenoxy]-4-methoxy-phenyl}-propionic acid benzyl ester
CAS No.:126383-90-2
Molecular Formula:C₄₉H₄₆N₂O₁₀
Molecular Weight:822.912
Hs Code.:

(S)-2-Benzyloxycarbonylamino-3-{3-[4-((S)-2-benzyloxycarbonyl-2-benzyloxycarbonylamino-ethyl)-phenoxy]-4-methoxy-phenyl}-propionic acid benzyl ester

Synonyms:(S)-2-Benzyloxycarbonylamino-3-{3-[4-((S)-2-benzyloxycarbonyl-2-benzyloxycarbonylamino-ethyl)-phenoxy]-4-methoxy-phenyl}-propionic acid benzyl ester

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Chemical Property of (S)-2-Benzyloxycarbonylamino-3-{3-[4-((S)-2-benzyloxycarbonyl-2-benzyloxycarbonylamino-ethyl)-phenoxy]-4-methoxy-phenyl}-propionic acid benzyl ester

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Technology Process of (S)-2-Benzyloxycarbonylamino-3-{3-[4-((S)-2-benzyloxycarbonyl-2-benzyloxycarbonylamino-ethyl)-phenoxy]-4-methoxy-phenyl}-propionic acid benzyl ester

There total 13 articles about (S)-2-Benzyloxycarbonylamino-3-{3-[4-((S)-2-benzyloxycarbonyl-2-benzyloxycarbonylamino-ethyl)-phenoxy]-4-methoxy-phenyl}-propionic acid benzyl 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:

: 100-39-0
benzyl bromide

: (S)-2-Benzyloxycarbonylamino-3-{3-[4-((S)-2-benzyloxycarbonylamino-2-carboxy-ethyl)-phenoxy]-4-methoxy-phenyl}-propionic acid

: 126383-90-2
(S)-2-Benzyloxycarbonylamino-3-{3-[4-((S)-2-benzyloxycarbonyl-2-benzyloxycarbonylamino-ethyl)-phenoxy]-4-methoxy-phenyl}-propionic acid benzyl ester

Guidance literature:: With CsCO₃; In N,N-dimethyl-formamide; at 25 ℃; for 1.5h; Yield given;
DOI:10.1016/S0040-4039(01)80692-4

Reference yield:

: 60-18-4,18875-48-4,25619-78-7,30704-25-7
L-tyrosine

: 126383-90-2
(S)-2-Benzyloxycarbonylamino-3-{3-[4-((S)-2-benzyloxycarbonyl-2-benzyloxycarbonylamino-ethyl)-phenoxy]-4-methoxy-phenyl}-propionic acid benzyl ester

Guidance literature:: Multi-step reaction with 8 steps

1: 96 percent / SOCl₂

2: 98 percent / K₂CO₃

3: 80 percent / NaBH₄, LiCl / tetrahydrofuran; diethyl ether

5: 6 N HCl

6: NaHCO₃

7: 15 h

8: CsCO₃ / dimethylformamide / 1.5 h / 25 °C

With hydrogenchloride; sodium tetrahydroborate; thionyl chloride; sodium hydrogencarbonate; potassium carbonate; lithium chloride; In tetrahydrofuran; diethyl ether; N,N-dimethyl-formamide;
DOI:10.1016/S0040-4039(01)80692-4

Reference yield:

: 6230-11-1
O-Methyltyrosine

: 126383-90-2
(S)-2-Benzyloxycarbonylamino-3-{3-[4-((S)-2-benzyloxycarbonyl-2-benzyloxycarbonylamino-ethyl)-phenoxy]-4-methoxy-phenyl}-propionic acid benzyl ester

Guidance literature:: Multi-step reaction with 8 steps

1: 82 percent / BH₃ / tetrahydrofuran

2: 70 percent / Br₂ / aq. formic acid

3: 86 percent / Na₂CO₃ / ethyl acetate; H₂O

5: 6 N HCl

6: NaHCO₃

7: 15 h

8: CsCO₃ / dimethylformamide / 1.5 h / 25 °C

With hydrogenchloride; borane; bromine; sodium hydrogencarbonate; sodium carbonate; In tetrahydrofuran; formic acid; water; ethyl acetate; N,N-dimethyl-formamide;
DOI:10.1016/S0040-4039(01)80692-4