3-benzyloxycarbonylamino-5-(tert-butoxycarbonyl-methyl-amino)-pentanoic acid tert-butyl ester

Base Information

Chemical Name:3-benzyloxycarbonylamino-5-(tert-butoxycarbonyl-methyl-amino)-pentanoic acid tert-butyl ester
CAS No.:868990-46-9
Molecular Formula:C₂₃H₃₆N₂O₆
Molecular Weight:436.549
Hs Code.:

3-benzyloxycarbonylamino-5-(<i>tert</i>-butoxycarbonyl-methyl-amino)-pentanoic acid <i>tert</i>-butyl ester

Synonyms:3-benzyloxycarbonylamino-5-(tert-butoxycarbonyl-methyl-amino)-pentanoic acid tert-butyl ester

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Chemical Property of 3-benzyloxycarbonylamino-5-(tert-butoxycarbonyl-methyl-amino)-pentanoic acid tert-butyl ester

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Technology Process of 3-benzyloxycarbonylamino-5-(tert-butoxycarbonyl-methyl-amino)-pentanoic acid tert-butyl ester

There total 8 articles about 3-benzyloxycarbonylamino-5-(tert-butoxycarbonyl-methyl-amino)-pentanoic 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:

: 868990-45-8
5-(tert-butoxycarbonyl-methyl-amino)-pent-2-enoic acid tert-butyl ester

: 868990-46-9
3-benzyloxycarbonylamino-5-(tert-butoxycarbonyl-methyl-amino)-pentanoic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 85 percent / n-BuLi

2: NH₄HCO₂ / Pd/C / Heating

3: NaHCO₃

With n-butyllithium; ammonium formate; sodium hydrogencarbonate; palladium on activated charcoal;
DOI:10.1002/jlcr.1242

Reference yield:

: 868990-44-7
3-[benzyl-(1-phenyl-ethyl)-amino]-5-(tert-butoxycarbonyl-methyl-amino)-pentanoic acid tert-butyl ester

: 868990-46-9
3-benzyloxycarbonylamino-5-(tert-butoxycarbonyl-methyl-amino)-pentanoic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: NH₄HCO₂ / Pd/C / Heating

2: NaHCO₃

With ammonium formate; sodium hydrogencarbonate; palladium on activated charcoal;
DOI:10.1002/jlcr.1242

Reference yield:

: 42116-55-2
methyl 3-tert-butoxycarbonylaminopropionate

: 868990-46-9
3-benzyloxycarbonylamino-5-(tert-butoxycarbonyl-methyl-amino)-pentanoic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 7 steps

1: 93 percent / NaH

2: 79 percent / DIBAL-H

3: DMSO; NEt₃; (COCl)2

4: 85 percent / n-BuLi

5: NH₄HCO₂ / Pd/C / Heating

6: NaHCO₃

With n-butyllithium; oxalyl dichloride; ammonium formate; sodium hydride; diisobutylaluminium hydride; sodium hydrogencarbonate; dimethyl sulfoxide; triethylamine; palladium on activated charcoal; 3: Swern oxidation / 4: Wadsworth-Emmons reaction;
DOI:10.1002/jlcr.1242