(R)-N-(5-(benzyloxy)thiazolo[5,4-b]pyridin-2-yl)-4H-1'-azaspiro[oxazole-5,3'-bicyclo[2.2.2]octan]-2-amine

Base Information

Chemical Name:(R)-N-(5-(benzyloxy)thiazolo[5,4-b]pyridin-2-yl)-4H-1'-azaspiro[oxazole-5,3'-bicyclo[2.2.2]octan]-2-amine
CAS No.:1192810-82-4
Molecular Formula:C₂₂H₂₃N₅O₂S
Molecular Weight:421.523
Hs Code.:

Synonyms:(R)-N-(5-(benzyloxy)thiazolo[5,4-b]pyridin-2-yl)-4H-1'-azaspiro[oxazole-5,3'-bicyclo[2.2.2]octan]-2-amine

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Chemical Property of (R)-N-(5-(benzyloxy)thiazolo[5,4-b]pyridin-2-yl)-4H-1'-azaspiro[oxazole-5,3'-bicyclo[2.2.2]octan]-2-amine

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Technology Process of (R)-N-(5-(benzyloxy)thiazolo[5,4-b]pyridin-2-yl)-4H-1'-azaspiro[oxazole-5,3'-bicyclo[2.2.2]octan]-2-amine

There total 4 articles about (R)-N-(5-(benzyloxy)thiazolo[5,4-b]pyridin-2-yl)-4H-1'-azaspiro[oxazole-5,3'-bicyclo[2.2.2]octan]-2-amine 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: 67.0%

: 1192814-04-2
dimethyl 5-(benzyloxy)thiazolo[5,4-b]pyridin-2-ylcarbonimidodithioate

: (S)-3-(aminomethyl)quinuclidin-3-ol dihydrochloride salt

: 1192810-82-4
(R)-N-(5-(benzyloxy)thiazolo[5,4-b]pyridin-2-yl)-4H-1'-azaspiro[oxazole-5,3'-bicyclo[2.2.2]octan]-2-amine

Guidance literature:: With caesium carbonate; In N,N-dimethyl-formamide; at 100 ℃; for 2h;

Reference yield:

: 128653-87-2
(3-(aminomethyl)-3-hydroxy-1-ammoniobicyclo[2.2.2]octan-1-yl)trihydroborate

: 1192810-82-4
(R)-N-(5-(benzyloxy)thiazolo[5,4-b]pyridin-2-yl)-4H-1'-azaspiro[oxazole-5,3'-bicyclo[2.2.2]octan]-2-amine

Guidance literature:: Multi-step reaction with 4 steps

1.1: sodium carbonate / dichloromethane / 0.67 h / 20 °C

2.1: carbon dioxide / acetonitrile; methanol

3.1: hydrogenchloride / water; acetone / 0.53 h / 20 °C / Cooling with ice

3.2: 20 °C

4.1: caesium carbonate / N,N-dimethyl-formamide / 2 h / 100 °C

With hydrogenchloride; carbon dioxide; sodium carbonate; caesium carbonate; In methanol; dichloromethane; water; N,N-dimethyl-formamide; acetone; acetonitrile;

Reference yield:

: 1192874-10-4,1192874-20-6,1192874-25-1
(3-((benzyloxycarbonylamino)methyl)-3-hydroxy-1-azabicyclo[2.2.2]octan-1-yl)trihydroborate

: 1192810-82-4
(R)-N-(5-(benzyloxy)thiazolo[5,4-b]pyridin-2-yl)-4H-1'-azaspiro[oxazole-5,3'-bicyclo[2.2.2]octan]-2-amine

Guidance literature:: Multi-step reaction with 3 steps

1.1: carbon dioxide / acetonitrile; methanol

2.1: hydrogenchloride / water; acetone / 0.53 h / 20 °C / Cooling with ice

2.2: 20 °C

3.1: caesium carbonate / N,N-dimethyl-formamide / 2 h / 100 °C

With hydrogenchloride; carbon dioxide; caesium carbonate; In methanol; water; N,N-dimethyl-formamide; acetone; acetonitrile;