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

Base Information

Chemical Name:(S)-2-[(3-{[(S)-3-(4-Benzyloxy-phenyl)-2-tert-butoxycarbonylamino-propyl]-hydroxy-carbamoyl}-propyl)-tert-butoxycarbonyl-amino]-pentanedioic acid dimethyl ester
CAS No.:215611-63-5
Molecular Formula:C₃₇H₅₃N₃O₁₁
Molecular Weight:715.841
Hs Code.:

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

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

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

: 215611-63-5
(S)-2-[(3-{[(S)-3-(4-Benzyloxy-phenyl)-2-tert-butoxycarbonylamino-propyl]-hydroxy-carbamoyl}-propyl)-tert-butoxycarbonyl-amino]-pentanedioic acid dimethyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: CH₂Cl₂ / 24 h / Ambient temperature

2: 76 percent / H₂ / 10percent Pd/C / ethyl acetate / 2 h

3: Et₃N / tetrahydrofuran / 0.5 h / 0 °C

4: tetrahydrofuran / 0.5 h / 0 °C

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:

: 23150-65-4
L-glutamic dimethyl ester hydrochloride

: 215611-63-5
(S)-2-[(3-{[(S)-3-(4-Benzyloxy-phenyl)-2-tert-butoxycarbonylamino-propyl]-hydroxy-carbamoyl}-propyl)-tert-butoxycarbonyl-amino]-pentanedioic acid dimethyl ester

Guidance literature:: Multi-step reaction with 6 steps

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

2: NaBH₄ / methanol / 0.5 h

3: CH₂Cl₂ / 24 h / Ambient temperature

4: 76 percent / H₂ / 10percent Pd/C / ethyl acetate / 2 h

5: Et₃N / tetrahydrofuran / 0.5 h / 0 °C

6: tetrahydrofuran / 0.5 h / 0 °C

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)-pentanedioic acid dimethyl ester

: 215611-63-5
(S)-2-[(3-{[(S)-3-(4-Benzyloxy-phenyl)-2-tert-butoxycarbonylamino-propyl]-hydroxy-carbamoyl}-propyl)-tert-butoxycarbonyl-amino]-pentanedioic acid dimethyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: CH₂Cl₂ / 24 h / Ambient temperature

2: 76 percent / H₂ / 10percent Pd/C / ethyl acetate / 2 h

3: Et₃N / tetrahydrofuran / 0.5 h / 0 °C

4: tetrahydrofuran / 0.5 h / 0 °C

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