N-(1-{[6-[bis-(4-methoxy-phenyl)-phenyl-methoxy]-8-(tert-butyl-dimethyl-silanyloxy)-2-oxa-bicyclo[3.2.1]oct-5-ylcarbamoyl]-methyl}-2-oxo-1,2-dihydro-pyrimidin-4-yl)-4-tert-butyl-benzamide

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Chemical Name:N-(1-{[6-[bis-(4-methoxy-phenyl)-phenyl-methoxy]-8-(tert-butyl-dimethyl-silanyloxy)-2-oxa-bicyclo[3.2.1]oct-5-ylcarbamoyl]-methyl}-2-oxo-1,2-dihydro-pyrimidin-4-yl)-4-tert-butyl-benzamide
CAS No.:512782-17-1
Molecular Formula:C₅₁H₆₂N₄O₈Si
Molecular Weight:887.161
Hs Code.:

<i>N</i>-(1-{[6-[bis-(4-methoxy-phenyl)-phenyl-methoxy]-8-(<i>tert</i>-butyl-dimethyl-silanyloxy)-2-oxa-bicyclo[3.2.1]oct-5-ylcarbamoyl]-methyl}-2-oxo-1,2-dihydro-pyrimidin-4-yl)-4-<i>tert</i>-butyl-benzamide

Synonyms:N-(1-{[6-[bis-(4-methoxy-phenyl)-phenyl-methoxy]-8-(tert-butyl-dimethyl-silanyloxy)-2-oxa-bicyclo[3.2.1]oct-5-ylcarbamoyl]-methyl}-2-oxo-1,2-dihydro-pyrimidin-4-yl)-4-tert-butyl-benzamide

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Chemical Property of N-(1-{[6-[bis-(4-methoxy-phenyl)-phenyl-methoxy]-8-(tert-butyl-dimethyl-silanyloxy)-2-oxa-bicyclo[3.2.1]oct-5-ylcarbamoyl]-methyl}-2-oxo-1,2-dihydro-pyrimidin-4-yl)-4-tert-butyl-benzamide

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Technology Process of N-(1-{[6-[bis-(4-methoxy-phenyl)-phenyl-methoxy]-8-(tert-butyl-dimethyl-silanyloxy)-2-oxa-bicyclo[3.2.1]oct-5-ylcarbamoyl]-methyl}-2-oxo-1,2-dihydro-pyrimidin-4-yl)-4-tert-butyl-benzamide

There total 3 articles about N-(1-{[6-[bis-(4-methoxy-phenyl)-phenyl-methoxy]-8-(tert-butyl-dimethyl-silanyloxy)-2-oxa-bicyclo[3.2.1]oct-5-ylcarbamoyl]-methyl}-2-oxo-1,2-dihydro-pyrimidin-4-yl)-4-tert-butyl-benzamide 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: 87.0%

: 239808-67-4
4,4’-dimethoxytrityl trifluoromethanesulfonate

: 4-tert-butyl-N-(1-{[8-(tert-butyl-dimethyl-silanyloxy)-6-hydroxy-2-oxa-bicyclo[3.2.1]oct-5-ylcarbamoyl]-methyl}-2-oxo-1,2-dihydro-pyrimidin-4-yl)-benzamide

: 512782-17-1
N-(1-{[6-[bis-(4-methoxy-phenyl)-phenyl-methoxy]-8-(tert-butyl-dimethyl-silanyloxy)-2-oxa-bicyclo[3.2.1]oct-5-ylcarbamoyl]-methyl}-2-oxo-1,2-dihydro-pyrimidin-4-yl)-4-tert-butyl-benzamide

Guidance literature:: With pyridine; at 60 ℃; for 5h;
DOI:10.1002/1521-3765(20021202)8:23<5312::AID-CHEM5312>3.0.CO;2-M

Reference yield:

: 172405-12-8
1-(carboxymethyl)-N⁴-(4-tert-butylbenzoyl)cytosine

: 512782-17-1
N-(1-{[6-[bis-(4-methoxy-phenyl)-phenyl-methoxy]-8-(tert-butyl-dimethyl-silanyloxy)-2-oxa-bicyclo[3.2.1]oct-5-ylcarbamoyl]-methyl}-2-oxo-1,2-dihydro-pyrimidin-4-yl)-4-tert-butyl-benzamide

Guidance literature:: Multi-step reaction with 2 steps

1: 88 percent / O-[(ethoxycarbonyl)cyanomethyleneamino]-N,N,N',N'-tetramethy; luronium tetrafluoroborate; (i-Pr)2NEt / dimethylformamide / 20 °C

2: 87 percent / pyridine / 5 h / 60 °C

With pyridine; luronium tetrafluoroborate; O-[(ethoxycarbonyl)cyanomethyleneamino]-N,N,N',N'-tetramethy; N-ethyl-N,N-diisopropylamine; In N,N-dimethyl-formamide;
DOI:10.1002/1521-3765(20021202)8:23<5312::AID-CHEM5312>3.0.CO;2-M

Reference yield:

: 206654-30-0
(1S,5S,6R,8S)-5-Amino-8-(tert-butyl-dimethyl-silanyloxy)-2-oxa-bicyclo[3.2.1]octan-6-ol

: 512782-17-1
N-(1-{[6-[bis-(4-methoxy-phenyl)-phenyl-methoxy]-8-(tert-butyl-dimethyl-silanyloxy)-2-oxa-bicyclo[3.2.1]oct-5-ylcarbamoyl]-methyl}-2-oxo-1,2-dihydro-pyrimidin-4-yl)-4-tert-butyl-benzamide

Guidance literature:: Multi-step reaction with 2 steps

1: 88 percent / O-[(ethoxycarbonyl)cyanomethyleneamino]-N,N,N',N'-tetramethy; luronium tetrafluoroborate; (i-Pr)2NEt / dimethylformamide / 20 °C

2: 87 percent / pyridine / 5 h / 60 °C

With pyridine; luronium tetrafluoroborate; O-[(ethoxycarbonyl)cyanomethyleneamino]-N,N,N',N'-tetramethy; N-ethyl-N,N-diisopropylamine; In N,N-dimethyl-formamide;
DOI:10.1002/1521-3765(20021202)8:23<5312::AID-CHEM5312>3.0.CO;2-M