L-N-Z-5-(benzyloxy)tryptophyl-N'-<2-(5-methoxy-3-indolyl)ethyl>glycinamide

Base Information

Chemical Name:L-N-Z-5-(benzyloxy)tryptophyl-N'-<2-(5-methoxy-3-indolyl)ethyl>glycinamide
CAS No.:150184-22-8
Molecular Formula:C₃₉H₃₉N₅O₆
Molecular Weight:673.769
Hs Code.:

Synonyms:L-N-Z-5-(benzyloxy)tryptophyl-N'-<2-(5-methoxy-3-indolyl)ethyl>glycinamide

Suppliers and Price of L-N-Z-5-(benzyloxy)tryptophyl-N'-<2-(5-methoxy-3-indolyl)ethyl>glycinamide

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

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Chemical Property of L-N-Z-5-(benzyloxy)tryptophyl-N'-<2-(5-methoxy-3-indolyl)ethyl>glycinamide

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Technology Process of L-N-Z-5-(benzyloxy)tryptophyl-N'-<2-(5-methoxy-3-indolyl)ethyl>glycinamide

There total 6 articles about L-N-Z-5-(benzyloxy)tryptophyl-N'-<2-(5-methoxy-3-indolyl)ethyl>glycinamide 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: 69.0%

: N'-<2-(5-methoxy-3-indolyl)ethyl>glycinamide hydrochloride

: 150184-19-3
L-N-benzyloxycarbonyl-5-benzyloxytryptophan pentachlorophenyl ester

: 150184-22-8
L-N-Z-5-(benzyloxy)tryptophyl-N'-<2-(5-methoxy-3-indolyl)ethyl>glycinamide

Guidance literature:: With triethylamine; In N,N-dimethyl-formamide; at 20 ℃; for 140h;

Reference yield:

: 3520-59-0
L-N-benzyloxycarbonyl-5-benzyloxytryptophan

: 150184-22-8
L-N-Z-5-(benzyloxy)tryptophyl-N'-<2-(5-methoxy-3-indolyl)ethyl>glycinamide

Guidance literature:: Multi-step reaction with 2 steps

1: 85 percent / dicyclohexylcarbodiimide / CH₂Cl₂ / 72 h / 5 °C

2: 69 percent / Et₃N / dimethylformamide / 140 h / 20 °C

With triethylamine; dicyclohexyl-carbodiimide; In dichloromethane; N,N-dimethyl-formamide;

Reference yield:

: 608-07-1
2-(5-methoxyindol-3-yl)ethylamine

: 150184-22-8
L-N-Z-5-(benzyloxy)tryptophyl-N'-<2-(5-methoxy-3-indolyl)ethyl>glycinamide

Guidance literature:: Multi-step reaction with 3 steps

1: ethyl acetate / 1.) -10 deg C, 1 h, 2.) from 18 deg C to 20 deg C, 24 h

2: 90 percent / HCl / diethyl ether / 24 h

3: 69 percent / Et₃N / dimethylformamide / 140 h / 20 °C

With hydrogenchloride; triethylamine; In diethyl ether; ethyl acetate; N,N-dimethyl-formamide;