N-<(1S)-(1-methoxycarbonyl-3-methylbutyl)carbamoyl>glycyl-L-valylglycyl-α-azanorvaline benzyl ester

Base Information

Chemical Name:N-<(1S)-(1-methoxycarbonyl-3-methylbutyl)carbamoyl>glycyl-L-valylglycyl-α-azanorvaline benzyl ester
CAS No.:112383-00-3
Molecular Formula:C₂₈H₄₄N₆O₈
Molecular Weight:592.693
Hs Code.:

Synonyms:N-<(1S)-(1-methoxycarbonyl-3-methylbutyl)carbamoyl>glycyl-L-valylglycyl-α-azanorvaline benzyl ester

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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 N-<(1S)-(1-methoxycarbonyl-3-methylbutyl)carbamoyl>glycyl-L-valylglycyl-α-azanorvaline benzyl ester

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Technology Process of N-<(1S)-(1-methoxycarbonyl-3-methylbutyl)carbamoyl>glycyl-L-valylglycyl-α-azanorvaline benzyl ester

There total 4 articles about N-<(1S)-(1-methoxycarbonyl-3-methylbutyl)carbamoyl>glycyl-L-valylglycyl-α-azanorvaline benzyl 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: 87.1%

: 112383-27-4
Gly-Val-Gly-Aznva-OCH₂Ph*HCl

: 30293-88-0,56753-77-6,39570-63-3
N-carbonyl-L-leucine methyl ester

: 112383-00-3
N-<(1S)-(1-methoxycarbonyl-3-methylbutyl)carbamoyl>glycyl-L-valylglycyl-α-azanorvaline benzyl ester

Guidance literature:: With triethylamine; In chloroform; for 4h;

Reference yield:

: 109953-68-6
α-azanorvaline benzyl ester

: 112383-00-3
N-<(1S)-(1-methoxycarbonyl-3-methylbutyl)carbamoyl>glycyl-L-valylglycyl-α-azanorvaline benzyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 97 percent / dicyclohexylcarbodi-imide, 1-hydroxybenzotriazole

2: HCl / ethyl acetate / 45 h / Ambient temperature

3: 87.1 percent / triethylamine / CHCl₃ / 4 h

With hydrogenchloride; benzotriazol-1-ol; triethylamine; dicyclohexyl-carbodiimide; In chloroform; ethyl acetate;

Reference yield:

: 112382-99-7
N-t-butoxycarbonylglycyl-L-valylglycyl-α-azanorvaline benzyl ester

: 112383-00-3
N-<(1S)-(1-methoxycarbonyl-3-methylbutyl)carbamoyl>glycyl-L-valylglycyl-α-azanorvaline benzyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: HCl / ethyl acetate / 45 h / Ambient temperature

2: 87.1 percent / triethylamine / CHCl₃ / 4 h

With hydrogenchloride; triethylamine; In chloroform; ethyl acetate;