3-(4-tert-butoxycarbonylamino-1H-indol-3-yl)-2-phenylacetylamino-propionic acid

Base Information

Chemical Name:3-(4-tert-butoxycarbonylamino-1H-indol-3-yl)-2-phenylacetylamino-propionic acid
CAS No.:319921-63-6
Molecular Formula:C₂₄H₂₇N₃O₅
Molecular Weight:437.495
Hs Code.:

3-(4-<i>tert</i>-butoxycarbonylamino-1<i>H</i>-indol-3-yl)-2-phenylacetylamino-propionic acid

Synonyms:3-(4-tert-butoxycarbonylamino-1H-indol-3-yl)-2-phenylacetylamino-propionic acid

Suppliers and Price of 3-(4-tert-butoxycarbonylamino-1H-indol-3-yl)-2-phenylacetylamino-propionic acid

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Total 1 raw suppliers

Chemical Property of 3-(4-tert-butoxycarbonylamino-1H-indol-3-yl)-2-phenylacetylamino-propionic acid

Chemical Property:

Purity/Quality:: 98% ^*data from raw suppliers

Safty Information:

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Technology Process of 3-(4-tert-butoxycarbonylamino-1H-indol-3-yl)-2-phenylacetylamino-propionic acid

There total 11 articles about 3-(4-tert-butoxycarbonylamino-1H-indol-3-yl)-2-phenylacetylamino-propionic 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: 39.0%

: 252288-57-6
4-(N-tert-Butyloxycarbonyl)amino-N-phenylacetyltryptophan

: 252288-58-7
(S)-4-(N-tert-Butyloxycarbonyl)aminotryptophan

: 319921-63-6
3-(4-tert-butoxycarbonylamino-1H-indol-3-yl)-2-phenylacetylamino-propionic acid

Guidance literature:: With methanol; water; penicillin G acyalse; at 37 ℃;
DOI:10.1002/(SICI)1521-3773(19991004)38:19<2902::AID-ANIE2902>3.0.CO;2-2

Reference yield:

: 146886-51-3
1-(N-triisopropylsilyl-1H-indol-3-yl)-N,N-dimethylmethanamine

: 319921-63-6
3-(4-tert-butoxycarbonylamino-1H-indol-3-yl)-2-phenylacetylamino-propionic acid

Guidance literature:: Multi-step reaction with 7 steps

1.1: tBuLi / diethyl ether / 1.75 h / -78 - 0 °C

1.2: 73 percent / diethyl ether / 1 h / -78 °C

2.1: 91.7 percent / tetrahydrofuran / 20 °C

3.1: MeI / dimethylformamide / 20 °C

4.1: 6.51 g / TBAF / tetrahydrofuran / 1 h / 20 °C

5.1: morpholine / Pd[PPh₃]4 / tetrahydrofuran / 0.5 h / 20 °C

6.1: 3.42 g / dioxane / 0.5 h / Heating

7.1: aq. NaOH; penicillin G acylase / aq. methanol / 37 °C / pH 7.6

With morpholine; sodium hydroxide; penicillin G acylase; tetrabutyl ammonium fluoride; tert.-butyl lithium; methyl iodide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In tetrahydrofuran; 1,4-dioxane; methanol; diethyl ether; N,N-dimethyl-formamide; 4.1: Mannich-type reaction;
DOI:10.1002/1521-3765(20001103)6:21<3943::AID-CHEM3943<3.3.CO;2-K

Reference yield:

: 146886-61-5
3-Dimethylaminomethyl-4-amino-1-triisopropylsilylindole

: 319921-63-6
3-(4-tert-butoxycarbonylamino-1H-indol-3-yl)-2-phenylacetylamino-propionic acid

Guidance literature:: Multi-step reaction with 6 steps

1: 91.7 percent / tetrahydrofuran / 20 °C

2: MeI / dimethylformamide / 20 °C

3: 6.51 g / TBAF / tetrahydrofuran / 1 h / 20 °C

4: morpholine / Pd[PPh₃]4 / tetrahydrofuran / 0.5 h / 20 °C

5: 3.42 g / dioxane / 0.5 h / Heating

6: aq. NaOH; penicillin G acylase / aq. methanol / 37 °C / pH 7.6

With morpholine; sodium hydroxide; penicillin G acylase; tetrabutyl ammonium fluoride; methyl iodide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In tetrahydrofuran; 1,4-dioxane; methanol; N,N-dimethyl-formamide; 3: Mannich-type reaction;
DOI:10.1002/1521-3765(20001103)6:21<3943::AID-CHEM3943<3.3.CO;2-K