tert-butyl 5-(1-(benzyloxycarbonyl)piperidin-4-yl)-3,4-dihydroisoquinoline-2(1H)-carboxylate

Base Information

Chemical Name:tert-butyl 5-(1-(benzyloxycarbonyl)piperidin-4-yl)-3,4-dihydroisoquinoline-2(1H)-carboxylate
CAS No.:1430563-75-9
Molecular Formula:C₂₇H₃₄N₂O₄
Molecular Weight:450.578
Hs Code.:
Mol file:1430563-75-9.mol

Synonyms:tert-butyl 5-(1-(benzyloxycarbonyl)piperidin-4-yl)-3,4-dihydroisoquinoline-2(1H)-carboxylate

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Chemical Property of tert-butyl 5-(1-(benzyloxycarbonyl)piperidin-4-yl)-3,4-dihydroisoquinoline-2(1H)-carboxylate

Chemical Property:

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Technology Process of tert-butyl 5-(1-(benzyloxycarbonyl)piperidin-4-yl)-3,4-dihydroisoquinoline-2(1H)-carboxylate

There total 4 articles about tert-butyl 5-(1-(benzyloxycarbonyl)piperidin-4-yl)-3,4-dihydroisoquinoline-2(1H)-carboxylate 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:

: C₁₉H₂₆N₂O₂

: 501-53-1,94274-21-2
benzyl chloroformate

: 1430563-75-9
tert-butyl 5-(1-(benzyloxycarbonyl)piperidin-4-yl)-3,4-dihydroisoquinoline-2(1H)-carboxylate

Guidance literature:: With sodium hydrogencarbonate; In dichloromethane; for 0.166667h;

Reference yield:

: 215184-78-4
5-bromo-3,4-dihydro-1H-isoquinoline-2-carboxylic acid tert-butyl ester

: 1430563-75-9
tert-butyl 5-(1-(benzyloxycarbonyl)piperidin-4-yl)-3,4-dihydroisoquinoline-2(1H)-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1: lithium chloride; bis-triphenylphosphine-palladium(II) chloride / toluene / 72 h / 110 °C

2: lithium triethylborohydride / tetrahydrofuran / 3.5 h / 0 - 20 °C

3: sodium hydrogencarbonate / dichloromethane / 0.17 h

With bis-triphenylphosphine-palladium(II) chloride; lithium triethylborohydride; sodium hydrogencarbonate; lithium chloride; In tetrahydrofuran; dichloromethane; toluene;

Reference yield:

: 1430217-25-6
tert-butyl 5-(pyridin-4-yl)-3,4-dihydroisoquinoline-2(1H)-carboxylate

: 1430563-75-9
tert-butyl 5-(1-(benzyloxycarbonyl)piperidin-4-yl)-3,4-dihydroisoquinoline-2(1H)-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: lithium triethylborohydride / tetrahydrofuran / 3.5 h / 0 - 20 °C

2: sodium hydrogencarbonate / dichloromethane / 0.17 h

With lithium triethylborohydride; sodium hydrogencarbonate; In tetrahydrofuran; dichloromethane;