4-methyl -N--1-(1H-indol-3-ylmethyl)-1-methyl-2-oxoethyl>amino>carbonyl>glycyl>-L-aspartate

Base Information

Chemical Name:4-methyl -N--1-(1H-indol-3-ylmethyl)-1-methyl-2-oxoethyl>amino>carbonyl>glycyl>-L-aspartate
CAS No.:144876-87-9
Molecular Formula:C₂₈H₃₄N₆O₇
Molecular Weight:566.614
Hs Code.:

4-methyl <R-(R*,R*)>-N-<N-<<<2-<(2-amino-2-phenylethyl)amino>-1-(1H-indol-3-ylmethyl)-1-methyl-2-oxoethyl>amino>carbonyl>glycyl>-L-aspartate

Synonyms:4-methyl -N--1-(1H-indol-3-ylmethyl)-1-methyl-2-oxoethyl>amino>carbonyl>glycyl>-L-aspartate

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Chemical Property of 4-methyl -N--1-(1H-indol-3-ylmethyl)-1-methyl-2-oxoethyl>amino>carbonyl>glycyl>-L-aspartate

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Technology Process of 4-methyl -N--1-(1H-indol-3-ylmethyl)-1-methyl-2-oxoethyl>amino>carbonyl>glycyl>-L-aspartate

There total 7 articles about 4-methyl -N--1-(1H-indol-3-ylmethyl)-1-methyl-2-oxoethyl>amino>carbonyl>glycyl>-L-aspartate 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:

: 144876-83-5
4-methyl-1-(phenylmethyl) -N-amino>ethyl>amino>ethyl>amino>carbonyl>glycyl>-L-aspartate

: 144876-87-9
4-methyl -N--1-(1H-indol-3-ylmethyl)-1-methyl-2-oxoethyl>amino>carbonyl>glycyl>-L-aspartate

Guidance literature:: With hydrogen; palladium dihydroxide; In ethanol; at 25 ℃; for 12h; under 2327.2 Torr;
DOI:10.1016/S0040-4020(01)86596-0

Reference yield:

: 51298-61-4
(S)-1-benzyl 4-methyl 2-aminosuccinate

: 144876-87-9
4-methyl -N--1-(1H-indol-3-ylmethyl)-1-methyl-2-oxoethyl>amino>carbonyl>glycyl>-L-aspartate

Guidance literature:: Multi-step reaction with 2 steps

1: 77 percent / BOP, i-Pr₂NEt / dimethylformamide / 12 h / 25 °C

2: 1.1 g / H₂ / 20percent Pd(OH)2/C / ethanol / 12 h / 25 °C / 2327.2 Torr

With hydrogen; (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; N-ethyl-N,N-diisopropylamine; palladium dihydroxide; In ethanol; N,N-dimethyl-formamide;
DOI:10.1016/S0040-4020(01)86596-0

Reference yield:

: 134558-28-4
N-[(9H-fluoren-9-ylmethyloxy)-carbonyl]-α-methyl-DL-tryptophan

: 144876-87-9
4-methyl -N--1-(1H-indol-3-ylmethyl)-1-methyl-2-oxoethyl>amino>carbonyl>glycyl>-L-aspartate

Guidance literature:: Multi-step reaction with 6 steps

1: 1) hydroxybenzotriazole hydrate, dicyclohexylcarbodiimide / 1) THF, EtOAc, 25 deg C, 2 h, 2) 25 deg C, 17 h

2: 80 percent / piperidine / dimethylformamide / 17 h / 0 °C

3: 79 percent / toluene; tetrahydrofuran / 16 h / 80 - 100 °C

4: 92 percent / LiOH*H₂O / tetrahydrofuran; H₂O / 25 °C

5: 77 percent / BOP, i-Pr₂NEt / dimethylformamide / 12 h / 25 °C

6: 1.1 g / H₂ / 20percent Pd(OH)2/C / ethanol / 12 h / 25 °C / 2327.2 Torr

With piperidine; lithium hydroxide; hydrogen; (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; benzotriazol-1-ol; N-ethyl-N,N-diisopropylamine; dicyclohexyl-carbodiimide; palladium dihydroxide; In tetrahydrofuran; ethanol; water; N,N-dimethyl-formamide; toluene;
DOI:10.1016/S0040-4020(01)86596-0