(S)-3-Benzyloxy-2-[((2R,4R,5R,6R)-5-hydroxy-5,6-dimethyl-2-phenyl-[1,3]dioxane-4-carbonyl)-amino]-2-methyl-propionic acid

Base Information

Chemical Name:(S)-3-Benzyloxy-2-[((2R,4R,5R,6R)-5-hydroxy-5,6-dimethyl-2-phenyl-[1,3]dioxane-4-carbonyl)-amino]-2-methyl-propionic acid
CAS No.:197567-48-9
Molecular Formula:C₂₄H₂₉NO₇
Molecular Weight:443.497
Hs Code.:

Synonyms:(S)-3-Benzyloxy-2-[((2R,4R,5R,6R)-5-hydroxy-5,6-dimethyl-2-phenyl-[1,3]dioxane-4-carbonyl)-amino]-2-methyl-propionic acid

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Chemical Property of (S)-3-Benzyloxy-2-[((2R,4R,5R,6R)-5-hydroxy-5,6-dimethyl-2-phenyl-[1,3]dioxane-4-carbonyl)-amino]-2-methyl-propionic acid

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Technology Process of (S)-3-Benzyloxy-2-[((2R,4R,5R,6R)-5-hydroxy-5,6-dimethyl-2-phenyl-[1,3]dioxane-4-carbonyl)-amino]-2-methyl-propionic acid

There total 8 articles about (S)-3-Benzyloxy-2-[((2R,4R,5R,6R)-5-hydroxy-5,6-dimethyl-2-phenyl-[1,3]dioxane-4-carbonyl)-amino]-2-methyl-propionic acid 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: 71.0%

: 197567-47-8
(S)-3-Benzyloxy-2-[((2R,4R,5R,6R)-5-hydroxy-5,6-dimethyl-2-phenyl-[1,3]dioxane-4-carbonyl)-amino]-2-methyl-propionic acid methyl ester

: 197567-48-9
(S)-3-Benzyloxy-2-[((2R,4R,5R,6R)-5-hydroxy-5,6-dimethyl-2-phenyl-[1,3]dioxane-4-carbonyl)-amino]-2-methyl-propionic acid

Guidance literature:: With potassium hydroxide; In 1,4-dioxane; for 17.5h;
DOI:10.1016/S0040-4020(97)00877-6

Reference yield:

: 32453-67-1
5-deoxy-1,2-O-isopropylidene-α-D-erythro-pentofuranos-3-ulose

: 197567-48-9
(S)-3-Benzyloxy-2-[((2R,4R,5R,6R)-5-hydroxy-5,6-dimethyl-2-phenyl-[1,3]dioxane-4-carbonyl)-amino]-2-methyl-propionic acid

Guidance literature:: Multi-step reaction with 7 steps

1: diethyl ether / 0.33 h

2: 92 percent / HCl / CH₂Cl₂

3: 85 percent / pTsOH / CH₂Cl₂ / 20 h / Ambient temperature

4: 0.49 g / HgO, BF₃*Et₂O / tetrahydrofuran

5: NaHCO₃, KBr, TEMPO, NaOCl / CH₂Cl₂ / 1 h

6: 1.) HOBT, DCC / 1.) CH₂Cl₂, 2 h, 2.) CH₂Cl₂, room temperature, 3 d

7: 71 percent / KOH / dioxane / 17.5 h

With hydrogenchloride; 2,2,6,6-tetramethyl-piperidine-N-oxyl; potassium hydroxide; sodium hypochlorite; boron trifluoride diethyl etherate; sodium hydrogencarbonate; benzotriazol-1-ol; toluene-4-sulfonic acid; dicyclohexyl-carbodiimide; potassium bromide; mercury(II) oxide; In tetrahydrofuran; 1,4-dioxane; diethyl ether; dichloromethane;
DOI:10.1016/S0040-4020(97)00877-6

Reference yield:

: 104467-82-5
5-deoxy-1,2-O-ispropylidene-3=C-methyl-α-D-ribofuranose

: 197567-48-9
(S)-3-Benzyloxy-2-[((2R,4R,5R,6R)-5-hydroxy-5,6-dimethyl-2-phenyl-[1,3]dioxane-4-carbonyl)-amino]-2-methyl-propionic acid

Guidance literature:: Multi-step reaction with 6 steps

1: 92 percent / HCl / CH₂Cl₂

2: 85 percent / pTsOH / CH₂Cl₂ / 20 h / Ambient temperature

3: 0.49 g / HgO, BF₃*Et₂O / tetrahydrofuran

4: NaHCO₃, KBr, TEMPO, NaOCl / CH₂Cl₂ / 1 h

5: 1.) HOBT, DCC / 1.) CH₂Cl₂, 2 h, 2.) CH₂Cl₂, room temperature, 3 d

6: 71 percent / KOH / dioxane / 17.5 h

With hydrogenchloride; 2,2,6,6-tetramethyl-piperidine-N-oxyl; potassium hydroxide; sodium hypochlorite; boron trifluoride diethyl etherate; sodium hydrogencarbonate; benzotriazol-1-ol; toluene-4-sulfonic acid; dicyclohexyl-carbodiimide; potassium bromide; mercury(II) oxide; In tetrahydrofuran; 1,4-dioxane; dichloromethane;
DOI:10.1016/S0040-4020(97)00877-6