α-{[(benzyloxy)carbonyl]amino}-1-[(tert-butoxy)carbonyl]-1H-indole-4-propanoic acid

Base Information

Chemical Name:α-{[(benzyloxy)carbonyl]amino}-1-[(tert-butoxy)carbonyl]-1H-indole-4-propanoic acid
CAS No.:938185-79-6
Molecular Formula:C₂₄H₂₆N₂O₆
Molecular Weight:438.48
Hs Code.:

Synonyms:α-{[(benzyloxy)carbonyl]amino}-1-[(tert-butoxy)carbonyl]-1H-indole-4-propanoic acid

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Chemical Property of α-{[(benzyloxy)carbonyl]amino}-1-[(tert-butoxy)carbonyl]-1H-indole-4-propanoic acid

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Technology Process of α-{[(benzyloxy)carbonyl]amino}-1-[(tert-butoxy)carbonyl]-1H-indole-4-propanoic acid

There total 2 articles about α-{[(benzyloxy)carbonyl]amino}-1-[(tert-butoxy)carbonyl]-1H-indole-4-propanoic acid 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: 100.0%

: 938185-76-3
methyl α-{[(benzyloxy)carbonyl]amino}-1-[(tert-butoxy)carbonyl]-1H-indole-4-propanoate

: 938185-79-6
α-{[(benzyloxy)carbonyl]amino}-1-[(tert-butoxy)carbonyl]-1H-indole-4-propanoic acid

Guidance literature:: With lithium hydroxide; In tetrahydrofuran; water; at 20 ℃; for 1h;
DOI:10.1002/hlca.200790058

Reference yield:

: 460096-31-5
(Z)-N^α-benzyloxycarbonyl-Nⁱⁿ-tert-butyloxycarbonyl-2,3-dehydro-3-(indol-4'-yl)-alanine, methyl ester

: 938185-79-6
α-{[(benzyloxy)carbonyl]amino}-1-[(tert-butoxy)carbonyl]-1H-indole-4-propanoic acid

Guidance literature:: Multi-step reaction with 2 steps

1: 89 percent / Mg / methanol / 2 h / 20 °C

2: 100 percent / LiOH*H₂O / tetrahydrofuran; H₂O / 1 h / 20 °C

With lithium hydroxide; magnesium; In tetrahydrofuran; methanol; water;
DOI:10.1002/hlca.200790058

Reference yield:

: 938185-79-6
α-{[(benzyloxy)carbonyl]amino}-1-[(tert-butoxy)carbonyl]-1H-indole-4-propanoic acid

: α-(benzoylamino)-N,N-dimethyl-1H-indole-4-propanamide

Guidance literature:: Multi-step reaction with 4 steps

1: 93 percent / Et₃N / acetonitrile / 3 h / -10 - 0 °C

2: 93 percent / AcOH / 16 h / 100 °C

3: 96 percent / H₂ / Pd/C / methanol / 2 h / 20 °C / 760.05 Torr

4: 95 mg / K₂CO₃ / tetrahydrofuran / 1 h / 20 °C

With hydrogen; potassium carbonate; acetic acid; triethylamine; palladium on activated charcoal; In tetrahydrofuran; methanol; acetonitrile;
DOI:10.1002/hlca.200790058