3-{1-[2-(4-Chloro-phenyl)-2-hydroxy-ethyl]-piperidin-4-yl}-3,4-dihydro-benzo[e][1,3]oxazin-2-one

Base Information

Chemical Name:3-{1-[2-(4-Chloro-phenyl)-2-hydroxy-ethyl]-piperidin-4-yl}-3,4-dihydro-benzo[e][1,3]oxazin-2-one
CAS No.:98767-73-8
Molecular Formula:C₂₁H₂₃ClN₂O₃
Molecular Weight:386.878
Hs Code.:

Synonyms:3-{1-[2-(4-Chloro-phenyl)-2-hydroxy-ethyl]-piperidin-4-yl}-3,4-dihydro-benzo[e][1,3]oxazin-2-one

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Chemical Property of 3-{1-[2-(4-Chloro-phenyl)-2-hydroxy-ethyl]-piperidin-4-yl}-3,4-dihydro-benzo[e][1,3]oxazin-2-one

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Technology Process of 3-{1-[2-(4-Chloro-phenyl)-2-hydroxy-ethyl]-piperidin-4-yl}-3,4-dihydro-benzo[e][1,3]oxazin-2-one

There total 6 articles about 3-{1-[2-(4-Chloro-phenyl)-2-hydroxy-ethyl]-piperidin-4-yl}-3,4-dihydro-benzo[e][1,3]oxazin-2-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: 76.1%

: 98767-69-2
3-{1-[2-(4-Chloro-phenyl)-2-oxo-ethyl]-piperidin-4-yl}-3,4-dihydro-benzo[e][1,3]oxazin-2-one

: 98767-73-8
3-{1-[2-(4-Chloro-phenyl)-2-hydroxy-ethyl]-piperidin-4-yl}-3,4-dihydro-benzo[e][1,3]oxazin-2-one

Guidance literature:: With sodium tetrahydroborate; In methanol; 1) 0-10 deg C, 1 h; 2) room temp., overnight;
DOI:10.1248/cpb.33.1104

Reference yield:

: 1205-72-7
1-benzyl-4-amino-piperidine dihydrochloride

: 98767-73-8
3-{1-[2-(4-Chloro-phenyl)-2-hydroxy-ethyl]-piperidin-4-yl}-3,4-dihydro-benzo[e][1,3]oxazin-2-one

Guidance literature:: Multi-step reaction with 5 steps

1: 2) NaBH₄ / 1) methanol, room temp, 1 h; 2) room temp. 2 h

2: 77.3 percent / tetrahydrofuran / 0.5 h / Heating

3: 84.9 percent / hydrogen, 1N HCl / 10percent Pd-C / H₂O; methanol / 40 °C

4: 79.5 percent / TEA / methanol / 48 h / Ambient temperature

5: 76.1 percent / NaBH₄ / methanol / 1) 0-10 deg C, 1 h; 2) room temp., overnight

With hydrogenchloride; sodium tetrahydroborate; TEA; hydrogen; palladium on activated charcoal; In tetrahydrofuran; methanol; water;
DOI:10.1248/cpb.33.1104

Reference yield:

: 90-02-8
salicylaldehyde

: 98767-73-8
3-{1-[2-(4-Chloro-phenyl)-2-hydroxy-ethyl]-piperidin-4-yl}-3,4-dihydro-benzo[e][1,3]oxazin-2-one

Guidance literature:: Multi-step reaction with 5 steps

1: 2) NaBH₄ / 1) methanol, room temp, 1 h; 2) room temp. 2 h

2: 77.3 percent / tetrahydrofuran / 0.5 h / Heating

3: 84.9 percent / hydrogen, 1N HCl / 10percent Pd-C / H₂O; methanol / 40 °C

4: 79.5 percent / TEA / methanol / 48 h / Ambient temperature

5: 76.1 percent / NaBH₄ / methanol / 1) 0-10 deg C, 1 h; 2) room temp., overnight

With hydrogenchloride; sodium tetrahydroborate; TEA; hydrogen; palladium on activated charcoal; In tetrahydrofuran; methanol; water;
DOI:10.1248/cpb.33.1104