(R)-2-tert-Butoxycarbonylamino-pent-4-enoic acid 3-((S)-2-benzyloxycarbonylamino-4-methylsulfanyl-butyryloxy)-propyl ester

Base Information

Chemical Name:(R)-2-tert-Butoxycarbonylamino-pent-4-enoic acid 3-((S)-2-benzyloxycarbonylamino-4-methylsulfanyl-butyryloxy)-propyl ester
CAS No.:203920-17-6
Molecular Formula:C₂₆H₃₈N₂O₈S
Molecular Weight:538.662
Hs Code.:

Synonyms:(R)-2-tert-Butoxycarbonylamino-pent-4-enoic acid 3-((S)-2-benzyloxycarbonylamino-4-methylsulfanyl-butyryloxy)-propyl ester

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Chemical Property of (R)-2-tert-Butoxycarbonylamino-pent-4-enoic acid 3-((S)-2-benzyloxycarbonylamino-4-methylsulfanyl-butyryloxy)-propyl ester

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Technology Process of (R)-2-tert-Butoxycarbonylamino-pent-4-enoic acid 3-((S)-2-benzyloxycarbonylamino-4-methylsulfanyl-butyryloxy)-propyl ester

There total 6 articles about (R)-2-tert-Butoxycarbonylamino-pent-4-enoic acid 3-((S)-2-benzyloxycarbonylamino-4-methylsulfanyl-butyryloxy)-propyl 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: 84.0%

: 170899-08-8
N-(tert-butoxycarbonyl)-D-allylglycine

: 203920-16-5
(S)-2-Benzyloxycarbonylamino-4-methylsulfanyl-butyric acid 3-hydroxy-propyl ester

: 203920-17-6
(R)-2-tert-Butoxycarbonylamino-pent-4-enoic acid 3-((S)-2-benzyloxycarbonylamino-4-methylsulfanyl-butyryloxy)-propyl ester

Guidance literature:: With dmap; 4-(dimethylamino)pyridine hydrochloride; dicyclohexyl-carbodiimide; In dichloromethane; Heating;
DOI:10.1021/jo972133h

Reference yield:

: 54594-06-8
D-allylglycine

: 203920-17-6
(R)-2-tert-Butoxycarbonylamino-pent-4-enoic acid 3-((S)-2-benzyloxycarbonylamino-4-methylsulfanyl-butyryloxy)-propyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 61 percent / NaHCO₃ / dioxane; H₂O / 5 h

2: 84 percent / DCC, DMAP, DMAP*HCl / CH₂Cl₂ / Heating

With dmap; 4-(dimethylamino)pyridine hydrochloride; sodium hydrogencarbonate; dicyclohexyl-carbodiimide; In 1,4-dioxane; dichloromethane; water;
DOI:10.1021/jo972133h

Reference yield:

: 63-68-3,26062-47-5,58576-49-1
L-methionine

: 203920-17-6
(R)-2-tert-Butoxycarbonylamino-pent-4-enoic acid 3-((S)-2-benzyloxycarbonylamino-4-methylsulfanyl-butyryloxy)-propyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 63 percent / NaHCO₃ / H₂O / 2 h / Ambient temperature

2: 79 percent / DCC, DMAP, DMAP*HCl / CH₂Cl₂ / 6 h / Heating

3: 84 percent / DCC, DMAP, DMAP*HCl / CH₂Cl₂ / Heating

With dmap; 4-(dimethylamino)pyridine hydrochloride; sodium hydrogencarbonate; dicyclohexyl-carbodiimide; In dichloromethane; water;
DOI:10.1021/jo972133h