((4aR,8R,8aS)-7-Benzyloxy-8-hydroxy-2,2-dimethyl-4a,7,8,8a-tetrahydro-4H-1,3-dioxa-5,7-diaza-naphthalen-6-yl)-carbamic acid benzyl ester

Base Information

Chemical Name:((4aR,8R,8aS)-7-Benzyloxy-8-hydroxy-2,2-dimethyl-4a,7,8,8a-tetrahydro-4H-1,3-dioxa-5,7-diaza-naphthalen-6-yl)-carbamic acid benzyl ester
CAS No.:272106-58-8
Molecular Formula:C₂₃H₂₇N₃O₆
Molecular Weight:441.484
Hs Code.:

Synonyms:((4aR,8R,8aS)-7-Benzyloxy-8-hydroxy-2,2-dimethyl-4a,7,8,8a-tetrahydro-4H-1,3-dioxa-5,7-diaza-naphthalen-6-yl)-carbamic acid benzyl ester

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Chemical Property of ((4aR,8R,8aS)-7-Benzyloxy-8-hydroxy-2,2-dimethyl-4a,7,8,8a-tetrahydro-4H-1,3-dioxa-5,7-diaza-naphthalen-6-yl)-carbamic acid benzyl ester

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Technology Process of ((4aR,8R,8aS)-7-Benzyloxy-8-hydroxy-2,2-dimethyl-4a,7,8,8a-tetrahydro-4H-1,3-dioxa-5,7-diaza-naphthalen-6-yl)-carbamic acid benzyl ester

There total 4 articles about ((4aR,8R,8aS)-7-Benzyloxy-8-hydroxy-2,2-dimethyl-4a,7,8,8a-tetrahydro-4H-1,3-dioxa-5,7-diaza-naphthalen-6-yl)-carbamic acid 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: 75.0%

: 272106-57-7
C₂₃H₂₉N₃O₆

: 272106-58-8
((4aR,8R,8aS)-7-Benzyloxy-8-hydroxy-2,2-dimethyl-4a,7,8,8a-tetrahydro-4H-1,3-dioxa-5,7-diaza-naphthalen-6-yl)-carbamic acid benzyl ester

Guidance literature:: With Dess-Martin periodane; In dichloromethane; at 20 ℃; for 6h;
DOI:10.1021/jo9915574

Reference yield:

: 187972-12-9
1-benzyloxy-3-benzyloxycarbonylthiourea

: 272106-58-8
((4aR,8R,8aS)-7-Benzyloxy-8-hydroxy-2,2-dimethyl-4a,7,8,8a-tetrahydro-4H-1,3-dioxa-5,7-diaza-naphthalen-6-yl)-carbamic acid benzyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 87 percent / mercuric chloride; Et₃N / dimethylformamide / 24 h / 20 °C

2: 59 percent / n-Bu₄NF / tetrahydrofuran / 0.5 h / 25 °C

3: 75 percent / Dess-Martin reagent / CH₂Cl₂ / 6 h / 20 °C

With tetrabutyl ammonium fluoride; Dess-Martin periodane; triethylamine; mercury dichloride; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide; 1: Condensation / 2: desilylation / 3: Cyclization;
DOI:10.1021/jo9915574

Reference yield:

: (4R,5R)-4-(tert-Butyl-diphenyl-silanyloxymethyl)-2,2-dimethyl-[1,3]dioxan-5-ylamine

: 272106-58-8
((4aR,8R,8aS)-7-Benzyloxy-8-hydroxy-2,2-dimethyl-4a,7,8,8a-tetrahydro-4H-1,3-dioxa-5,7-diaza-naphthalen-6-yl)-carbamic acid benzyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 87 percent / mercuric chloride; Et₃N / dimethylformamide / 24 h / 20 °C

2: 59 percent / n-Bu₄NF / tetrahydrofuran / 0.5 h / 25 °C

3: 75 percent / Dess-Martin reagent / CH₂Cl₂ / 6 h / 20 °C

With tetrabutyl ammonium fluoride; Dess-Martin periodane; triethylamine; mercury dichloride; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide; 1: Condensation / 2: desilylation / 3: Cyclization;
DOI:10.1021/jo9915574