(1R,4R,5S)-8-(9H-fluoren-9-yl)methyloxycarbonyl-4-(benzyloxy)-2,3-(3'-fluorobenzo)-7-oxa-8-azabicyclo[3.2.1]octane

Base Information

Chemical Name:(1R,4R,5S)-8-(9H-fluoren-9-yl)methyloxycarbonyl-4-(benzyloxy)-2,3-(3'-fluorobenzo)-7-oxa-8-azabicyclo[3.2.1]octane
CAS No.:1307771-75-0
Molecular Formula:C₃₂H₂₆FNO₄
Molecular Weight:507.561
Hs Code.:

Synonyms:(1R,4R,5S)-8-(9H-fluoren-9-yl)methyloxycarbonyl-4-(benzyloxy)-2,3-(3'-fluorobenzo)-7-oxa-8-azabicyclo[3.2.1]octane

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Chemical Property of (1R,4R,5S)-8-(9H-fluoren-9-yl)methyloxycarbonyl-4-(benzyloxy)-2,3-(3'-fluorobenzo)-7-oxa-8-azabicyclo[3.2.1]octane

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Technology Process of (1R,4R,5S)-8-(9H-fluoren-9-yl)methyloxycarbonyl-4-(benzyloxy)-2,3-(3'-fluorobenzo)-7-oxa-8-azabicyclo[3.2.1]octane

There total 5 articles about (1R,4R,5S)-8-(9H-fluoren-9-yl)methyloxycarbonyl-4-(benzyloxy)-2,3-(3'-fluorobenzo)-7-oxa-8-azabicyclo[3.2.1]octane 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: 93.0%

: 1307771-43-2
((3S,4R)-4-(benzyloxy)-7-fluoro-3,4-dihydroisoquinolin-3-yl)methanol

: 28920-43-6
(fluorenylmethoxy)carbonyl chloride

: 1307771-75-0
(1R,4R,5S)-8-(9H-fluoren-9-yl)methyloxycarbonyl-4-(benzyloxy)-2,3-(3'-fluorobenzo)-7-oxa-8-azabicyclo[3.2.1]octane

Guidance literature:: In dichloromethane; at 20 ℃;
DOI:10.1002/chem.201002938

Reference yield:

: 1307771-17-0
tert-butyl (4S)-4-((R)-(2-(1,3-dioxan-2-yl)-4-fluorophenyl)(benzyloxy)methyl)-2,2-dimethyloxazolidine-3-carboxylate

: 1307771-75-0
(1R,4R,5S)-8-(9H-fluoren-9-yl)methyloxycarbonyl-4-(benzyloxy)-2,3-(3'-fluorobenzo)-7-oxa-8-azabicyclo[3.2.1]octane

Guidance literature:: Multi-step reaction with 2 steps

1: hydrogenchloride / tetrahydrofuran; water / 2 h / 20 °C

2: dichloromethane / 20 °C

With hydrogenchloride; In tetrahydrofuran; dichloromethane; water;
DOI:10.1002/chem.201002938

Reference yield:

: C₂₁H₃₀FNO₆

: 1307771-75-0
(1R,4R,5S)-8-(9H-fluoren-9-yl)methyloxycarbonyl-4-(benzyloxy)-2,3-(3'-fluorobenzo)-7-oxa-8-azabicyclo[3.2.1]octane

Guidance literature:: Multi-step reaction with 3 steps

1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 3 h / 0 °C

2: hydrogenchloride / tetrahydrofuran; water / 2 h / 20 °C

3: dichloromethane / 20 °C

With hydrogenchloride; sodium hydride; In tetrahydrofuran; dichloromethane; water; N,N-dimethyl-formamide; mineral oil;
DOI:10.1002/chem.201002938