tert-butyl 5-(benzyloxy)-6-methyl-2-[(piperidin-4-yl)methyl]pyrimidine-4-carboxylate hydrochloride

Base Information

Chemical Name:tert-butyl 5-(benzyloxy)-6-methyl-2-[(piperidin-4-yl)methyl]pyrimidine-4-carboxylate hydrochloride
CAS No.:1192164-03-6
Molecular Formula:C₂₃H₃₁N₃O₃*ClH
Molecular Weight:433.978
Hs Code.:

Synonyms:tert-butyl 5-(benzyloxy)-6-methyl-2-[(piperidin-4-yl)methyl]pyrimidine-4-carboxylate hydrochloride

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Chemical Property of tert-butyl 5-(benzyloxy)-6-methyl-2-[(piperidin-4-yl)methyl]pyrimidine-4-carboxylate hydrochloride

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Technology Process of tert-butyl 5-(benzyloxy)-6-methyl-2-[(piperidin-4-yl)methyl]pyrimidine-4-carboxylate hydrochloride

There total 6 articles about tert-butyl 5-(benzyloxy)-6-methyl-2-[(piperidin-4-yl)methyl]pyrimidine-4-carboxylate hydrochloride 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: 95.0%

: 1192164-02-5
tert-butyl 5-(benzyloxy)-2-{[1-(tert-butoxycarbonyl)piperidin-4-yl]methyl}-6-methylpyrimidine-4-carboxylate

: 1192164-03-6
tert-butyl 5-(benzyloxy)-6-methyl-2-[(piperidin-4-yl)methyl]pyrimidine-4-carboxylate hydrochloride

Guidance literature:: With hydrogenchloride; In ethyl acetate; at 20 ℃; for 3h;

Reference yield:

: 1192163-99-7
tert-butyl 5-(benzyloxy)-2-{[1-(tert-butoxycarbonyl)piperidin-4-yl]methyl}-6-hydroxypyrimidine-4-carboxylate

: 1192164-03-6
tert-butyl 5-(benzyloxy)-6-methyl-2-[(piperidin-4-yl)methyl]pyrimidine-4-carboxylate hydrochloride

Guidance literature:: Multi-step reaction with 3 steps

1: triethylamine / dichloromethane / 0.5 h / -78 °C

2: potassium carbonate; silver(l) oxide / dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂ / tetrahydrofuran / 3 h / Inert atmosphere; Reflux

3: hydrogenchloride / ethyl acetate / 3 h / 20 °C

With hydrogenchloride; potassium carbonate; triethylamine; silver(l) oxide; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; In tetrahydrofuran; dichloromethane; ethyl acetate;

Reference yield:

: 1192164-01-4
tert-butyl 5-(benzyloxy)-2-{[1-(tert-butoxycarbonyl)piperidin-4-yl]methyl}-6-{[(trifluoromethyl)sulfonyl]oxy}pyrimidine-4-carboxylate

: 1192164-03-6
tert-butyl 5-(benzyloxy)-6-methyl-2-[(piperidin-4-yl)methyl]pyrimidine-4-carboxylate hydrochloride

Guidance literature:: Multi-step reaction with 2 steps

1: potassium carbonate; silver(l) oxide / dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂ / tetrahydrofuran / 3 h / Inert atmosphere; Reflux

2: hydrogenchloride / ethyl acetate / 3 h / 20 °C

With hydrogenchloride; potassium carbonate; silver(l) oxide; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; In tetrahydrofuran; ethyl acetate;