(S)-3-(4-Hydroxy-phenyl)-2-[(S)-2-(6-iodo-hexanoylamino)-3-methyl-butyrylamino]-propionic acid benzyl ester

Base Information

Chemical Name:(S)-3-(4-Hydroxy-phenyl)-2-[(S)-2-(6-iodo-hexanoylamino)-3-methyl-butyrylamino]-propionic acid benzyl ester
CAS No.:437754-03-5
Molecular Formula:C₂₇H₃₅IN₂O₅
Molecular Weight:594.49
Hs Code.:

Synonyms:(S)-3-(4-Hydroxy-phenyl)-2-[(S)-2-(6-iodo-hexanoylamino)-3-methyl-butyrylamino]-propionic acid benzyl ester

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Chemical Property of (S)-3-(4-Hydroxy-phenyl)-2-[(S)-2-(6-iodo-hexanoylamino)-3-methyl-butyrylamino]-propionic acid benzyl ester

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Technology Process of (S)-3-(4-Hydroxy-phenyl)-2-[(S)-2-(6-iodo-hexanoylamino)-3-methyl-butyrylamino]-propionic acid benzyl ester

There total 5 articles about (S)-3-(4-Hydroxy-phenyl)-2-[(S)-2-(6-iodo-hexanoylamino)-3-methyl-butyrylamino]-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:

: 180078-20-0
6-bromohexanoyl-L-valinyl-L-tyrosine benzyl ester

: 437754-03-5
(S)-3-(4-Hydroxy-phenyl)-2-[(S)-2-(6-iodo-hexanoylamino)-3-methyl-butyrylamino]-propionic acid benzyl ester

Guidance literature:: With sodium iodide; In acetone; at 20 ℃;
DOI:10.1021/ja0256461

Reference yield:

: 13734-41-3
t-Boc-L-valine

: 437754-03-5
(S)-3-(4-Hydroxy-phenyl)-2-[(S)-2-(6-iodo-hexanoylamino)-3-methyl-butyrylamino]-propionic acid benzyl ester

Guidance literature:: Multi-step reaction with 4 steps

1.1: isobutyl chloroformate; N-methyl morpholine / tetrahydrofuran / 0.08 h / -10 °C

1.2: 98 percent / HOBt; N-methyl morpholine / CH₂Cl₂; tetrahydrofuran / 3 h / 20 °C

2.1: TFA / 0.25 h

3.1: 5.1 g / aq. K₂CO₃ / tetrahydrofuran / 0.5 h / 20 °C / pH 9

4.1: NaI / acetone / 20 °C

With 4-methyl-morpholine; potassium carbonate; trifluoroacetic acid; sodium iodide; isobutyl chloroformate; In tetrahydrofuran; acetone;
DOI:10.1021/ja0256461

Reference yield:

: 42406-77-9
L-tyrosine benzyl ester

: 437754-03-5
(S)-3-(4-Hydroxy-phenyl)-2-[(S)-2-(6-iodo-hexanoylamino)-3-methyl-butyrylamino]-propionic acid benzyl ester

Guidance literature:: Multi-step reaction with 4 steps

1.1: isobutyl chloroformate; N-methyl morpholine / tetrahydrofuran / 0.08 h / -10 °C

1.2: 98 percent / HOBt; N-methyl morpholine / CH₂Cl₂; tetrahydrofuran / 3 h / 20 °C

2.1: TFA / 0.25 h

3.1: 5.1 g / aq. K₂CO₃ / tetrahydrofuran / 0.5 h / 20 °C / pH 9

4.1: NaI / acetone / 20 °C

With 4-methyl-morpholine; potassium carbonate; trifluoroacetic acid; sodium iodide; isobutyl chloroformate; In tetrahydrofuran; acetone;
DOI:10.1021/ja0256461