(1S,4S,5R,6S,7S)-N-(p-anisyldiphenylmethyl)-2-azabicyclo[2.2.1]heptan-7-bromo-5,6-diol-3-one

Base Information

Chemical Name:(1S,4S,5R,6S,7S)-N-(p-anisyldiphenylmethyl)-2-azabicyclo[2.2.1]heptan-7-bromo-5,6-diol-3-one
CAS No.:913648-80-3
Molecular Formula:C₂₆H₂₄BrNO₄
Molecular Weight:494.385
Hs Code.:

Synonyms:(1S,4S,5R,6S,7S)-N-(p-anisyldiphenylmethyl)-2-azabicyclo[2.2.1]heptan-7-bromo-5,6-diol-3-one

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (1S,4S,5R,6S,7S)-N-(p-anisyldiphenylmethyl)-2-azabicyclo[2.2.1]heptan-7-bromo-5,6-diol-3-one

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Technology Process of (1S,4S,5R,6S,7S)-N-(p-anisyldiphenylmethyl)-2-azabicyclo[2.2.1]heptan-7-bromo-5,6-diol-3-one

There total 5 articles about (1S,4S,5R,6S,7S)-N-(p-anisyldiphenylmethyl)-2-azabicyclo[2.2.1]heptan-7-bromo-5,6-diol-3-one 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: 90.0%

: 913648-77-8
(1S,4S,7S)-N-(p-anisyldiphenylmethyl)-2-azabicyclo[2.2.1]hept-7-bromo-5-en-3-one

: 913648-80-3
(1S,4S,5R,6S,7S)-N-(p-anisyldiphenylmethyl)-2-azabicyclo[2.2.1]heptan-7-bromo-5,6-diol-3-one

Guidance literature:: With osmium(VIII) oxide; 4-methylmorpholine N-oxide; In water; acetone; tert-butyl alcohol; for 24h; Heating;
DOI:10.1021/jo060920l

Reference yield:

: 913648-69-8
(1S,4R)-N-(p-anisyldiphenylmethyl)-2-azabicyclo[2.2.1]hept-5-en-3-one

: 913648-80-3
(1S,4S,5R,6S,7S)-N-(p-anisyldiphenylmethyl)-2-azabicyclo[2.2.1]heptan-7-bromo-5,6-diol-3-one

Guidance literature:: Multi-step reaction with 3 steps

1: 70.5 percent / magnesium oxide; bromine / CCl₄ / 18 h / 20 °C

2: 84 percent / 1,8-diazabicycloundecene / 18 h / 125 °C

3: 90 percent / N-methylmorpholine-N-oxide; OsO₄ / acetone; H₂O; 2-methyl-propan-2-ol / 24 h / Heating

With osmium(VIII) oxide; 1,8-diazabicycloundecene; bromine; magnesium oxide; 4-methylmorpholine N-oxide; In tetrachloromethane; water; acetone; tert-butyl alcohol;
DOI:10.1021/jo060920l

Reference yield:

: 913648-72-3
(1S,4S,6R,7S)-N-(p-anisyldiphenylmethyl)-2-azabicyclo[2.2.1]heptan-6,7-dibromo-3-one

: 913648-80-3
(1S,4S,5R,6S,7S)-N-(p-anisyldiphenylmethyl)-2-azabicyclo[2.2.1]heptan-7-bromo-5,6-diol-3-one

Guidance literature:: Multi-step reaction with 2 steps

1: 84 percent / 1,8-diazabicycloundecene / 18 h / 125 °C

2: 90 percent / N-methylmorpholine-N-oxide; OsO₄ / acetone; H₂O; 2-methyl-propan-2-ol / 24 h / Heating

With osmium(VIII) oxide; 1,8-diazabicycloundecene; 4-methylmorpholine N-oxide; In water; acetone; tert-butyl alcohol;
DOI:10.1021/jo060920l