(S)-2-[(3-{[(S)-3-(4-Benzyloxy-phenyl)-2-tert-butoxycarbonylamino-propyl]-hydroxy-carbamoyl}-propyl)-tert-butoxycarbonyl-amino]-6-tert-butoxycarbonylamino-hexanoic acid methyl ester

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Chemical Name:(S)-2-[(3-{[(S)-3-(4-Benzyloxy-phenyl)-2-tert-butoxycarbonylamino-propyl]-hydroxy-carbamoyl}-propyl)-tert-butoxycarbonyl-amino]-6-tert-butoxycarbonylamino-hexanoic acid methyl ester
CAS No.:215611-65-7
Molecular Formula:C₄₂H₆₄N₄O₁₁
Molecular Weight:800.99
Hs Code.:

(S)-2-[(3-{[(S)-3-(4-Benzyloxy-phenyl)-2-tert-butoxycarbonylamino-propyl]-hydroxy-carbamoyl}-propyl)-tert-butoxycarbonyl-amino]-6-tert-butoxycarbonylamino-hexanoic acid methyl ester

Synonyms:(S)-2-[(3-{[(S)-3-(4-Benzyloxy-phenyl)-2-tert-butoxycarbonylamino-propyl]-hydroxy-carbamoyl}-propyl)-tert-butoxycarbonyl-amino]-6-tert-butoxycarbonylamino-hexanoic acid methyl ester

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Chemical Property of (S)-2-[(3-{[(S)-3-(4-Benzyloxy-phenyl)-2-tert-butoxycarbonylamino-propyl]-hydroxy-carbamoyl}-propyl)-tert-butoxycarbonyl-amino]-6-tert-butoxycarbonylamino-hexanoic acid methyl ester

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Technology Process of (S)-2-[(3-{[(S)-3-(4-Benzyloxy-phenyl)-2-tert-butoxycarbonylamino-propyl]-hydroxy-carbamoyl}-propyl)-tert-butoxycarbonyl-amino]-6-tert-butoxycarbonylamino-hexanoic acid methyl ester

There total 7 articles about (S)-2-[(3-{[(S)-3-(4-Benzyloxy-phenyl)-2-tert-butoxycarbonylamino-propyl]-hydroxy-carbamoyl}-propyl)-tert-butoxycarbonyl-amino]-6-tert-butoxycarbonylamino-hexanoic acid methyl 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:

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

: 215611-65-7
(S)-2-[(3-{[(S)-3-(4-Benzyloxy-phenyl)-2-tert-butoxycarbonylamino-propyl]-hydroxy-carbamoyl}-propyl)-tert-butoxycarbonyl-amino]-6-tert-butoxycarbonylamino-hexanoic acid methyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: CH₂Cl₂ / Ambient temperature

2: 89 percent / H₂ / 10percent Pd/C / ethyl acetate / 2 h

3: Et₃N / tetrahydrofuran / 0 °C

4: tetrahydrofuran / 0.5 h

With hydrogen; triethylamine; palladium on activated charcoal; In tetrahydrofuran; dichloromethane; ethyl acetate;
DOI:10.1002/(SICI)1521-3765(19980904)4:9<1698::AID-CHEM1698>3.0.CO;2-J

Reference yield:

: 2389-48-2
N-ε-tert-butoxycarbonyl-L-lysine methyl ester hydrochloride

: 215611-65-7
(S)-2-[(3-{[(S)-3-(4-Benzyloxy-phenyl)-2-tert-butoxycarbonylamino-propyl]-hydroxy-carbamoyl}-propyl)-tert-butoxycarbonyl-amino]-6-tert-butoxycarbonylamino-hexanoic acid methyl ester

Guidance literature:: Multi-step reaction with 6 steps

1: Et₃N, MgSO₄ / CH₂Cl₂ / 2 h / Ambient temperature

2: NaBH₄ / methanol / 0.5 h / 0 °C

3: CH₂Cl₂ / Ambient temperature

4: 89 percent / H₂ / 10percent Pd/C / ethyl acetate / 2 h

5: Et₃N / tetrahydrofuran / 0 °C

6: tetrahydrofuran / 0.5 h

With sodium tetrahydroborate; hydrogen; magnesium sulfate; triethylamine; palladium on activated charcoal; In tetrahydrofuran; methanol; dichloromethane; ethyl acetate;
DOI:10.1002/(SICI)1521-3765(19980904)4:9<1698::AID-CHEM1698>3.0.CO;2-J

Reference yield:

: (S)-2-(3-Benzyloxycarbonyl-propylamino)-6-tert-butoxycarbonylamino-hexanoic acid methyl ester

: 215611-65-7
(S)-2-[(3-{[(S)-3-(4-Benzyloxy-phenyl)-2-tert-butoxycarbonylamino-propyl]-hydroxy-carbamoyl}-propyl)-tert-butoxycarbonyl-amino]-6-tert-butoxycarbonylamino-hexanoic acid methyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: CH₂Cl₂ / Ambient temperature

2: 89 percent / H₂ / 10percent Pd/C / ethyl acetate / 2 h

3: Et₃N / tetrahydrofuran / 0 °C

4: tetrahydrofuran / 0.5 h

With hydrogen; triethylamine; palladium on activated charcoal; In tetrahydrofuran; dichloromethane; ethyl acetate;
DOI:10.1002/(SICI)1521-3765(19980904)4:9<1698::AID-CHEM1698>3.0.CO;2-J