4-(L-tyrosylamino)-1-(N-acetyl-L-phenylalanyl)piperidine hydrochloride

Base Information

Chemical Name:4-(L-tyrosylamino)-1-(N-acetyl-L-phenylalanyl)piperidine hydrochloride
CAS No.:120687-41-4
Molecular Formula:C₂₅H₃₂N₄O₄*ClH
Molecular Weight:489.014
Hs Code.:

Synonyms:4-(L-tyrosylamino)-1-(N-acetyl-L-phenylalanyl)piperidine hydrochloride

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Chemical Property of 4-(L-tyrosylamino)-1-(N-acetyl-L-phenylalanyl)piperidine hydrochloride

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Technology Process of 4-(L-tyrosylamino)-1-(N-acetyl-L-phenylalanyl)piperidine hydrochloride

There total 5 articles about 4-(L-tyrosylamino)-1-(N-acetyl-L-phenylalanyl)piperidine hydrochloride 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: 38.0%

: 120687-48-1
4-(BOC-tyrosylamino)-1-(N-acetyl-L-phenylalanyl)piperidine

: 120687-41-4
4-(L-tyrosylamino)-1-(N-acetyl-L-phenylalanyl)piperidine hydrochloride

Guidance literature:: With hydrogenchloride; In 1,4-dioxane; Ambient temperature;
DOI:10.1021/jm00128a007

Reference yield:

: 50541-93-0
4-amino-1-benzylpiperidine

: 120687-41-4
4-(L-tyrosylamino)-1-(N-acetyl-L-phenylalanyl)piperidine hydrochloride

Guidance literature:: Multi-step reaction with 4 steps

1: 1-hydroxybenztriazole, N,N'-dicyclohexylcarbodiimide / CH₂Cl₂ / Ambient temperature

2: 87 percent / H₂ / 10percent Pd/C / ethanol / 8 h / 760 Torr / Heating

3: 56 percent / N,N'-dicyclohexylcarbodiimide, 1-hydroxybenzotriazole, Et₃N / CHCl₃

4: 38 percent / 4N aq. HCl / dioxane / Ambient temperature

With hydrogenchloride; hydrogen; benzotriazol-1-ol; triethylamine; dicyclohexyl-carbodiimide; palladium on activated charcoal; In 1,4-dioxane; ethanol; dichloromethane; chloroform;
DOI:10.1021/jm00128a007

Reference yield:

: 3978-80-1
Boc-Tyr-OH

: 120687-41-4
4-(L-tyrosylamino)-1-(N-acetyl-L-phenylalanyl)piperidine hydrochloride

Guidance literature:: Multi-step reaction with 4 steps

1: 1-hydroxybenztriazole, N,N'-dicyclohexylcarbodiimide / CH₂Cl₂ / Ambient temperature

2: 87 percent / H₂ / 10percent Pd/C / ethanol / 8 h / 760 Torr / Heating

3: 56 percent / N,N'-dicyclohexylcarbodiimide, 1-hydroxybenzotriazole, Et₃N / CHCl₃

4: 38 percent / 4N aq. HCl / dioxane / Ambient temperature

With hydrogenchloride; hydrogen; benzotriazol-1-ol; triethylamine; dicyclohexyl-carbodiimide; palladium on activated charcoal; In 1,4-dioxane; ethanol; dichloromethane; chloroform;
DOI:10.1021/jm00128a007