2-[2-(1-benzyl-6-oxo-1,4,5,6-tetrahydro-pyridin-3-yl)-2-hydroxy-ethyl]-piperidine-1-carboxylic acid tert-butyl ester

Base Information

Chemical Name:2-[2-(1-benzyl-6-oxo-1,4,5,6-tetrahydro-pyridin-3-yl)-2-hydroxy-ethyl]-piperidine-1-carboxylic acid tert-butyl ester
CAS No.:460997-30-2
Molecular Formula:C₂₄H₃₄N₂O₄
Molecular Weight:414.545
Hs Code.:

2-[2-(1-benzyl-6-oxo-1,4,5,6-tetrahydro-pyridin-3-yl)-2-hydroxy-ethyl]-piperidine-1-carboxylic acid <i>tert</i>-butyl ester

Synonyms:2-[2-(1-benzyl-6-oxo-1,4,5,6-tetrahydro-pyridin-3-yl)-2-hydroxy-ethyl]-piperidine-1-carboxylic acid tert-butyl ester

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Chemical Property of 2-[2-(1-benzyl-6-oxo-1,4,5,6-tetrahydro-pyridin-3-yl)-2-hydroxy-ethyl]-piperidine-1-carboxylic acid tert-butyl ester

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Technology Process of 2-[2-(1-benzyl-6-oxo-1,4,5,6-tetrahydro-pyridin-3-yl)-2-hydroxy-ethyl]-piperidine-1-carboxylic acid tert-butyl ester

There total 11 articles about 2-[2-(1-benzyl-6-oxo-1,4,5,6-tetrahydro-pyridin-3-yl)-2-hydroxy-ethyl]-piperidine-1-carboxylic acid tert-butyl ester 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:

: 460997-29-9
2-[(1-benzyl-6-oxo-1,4,5,6-tetrahydro-pyridin-3-yl)-2-oxo-ethyl]-piperidine-1-carboxylic acid tert-butyl ester

: 460997-30-2
2-[2-(1-benzyl-6-oxo-1,4,5,6-tetrahydro-pyridin-3-yl)-2-hydroxy-ethyl]-piperidine-1-carboxylic acid tert-butyl ester

Guidance literature:: With sodium tetrahydroborate; In tetrahydrofuran; methanol; at 0 ℃; for 2h;
DOI:10.1021/ol0263144

Reference yield:

: 1484-84-0
2(RS)-(2-hydroxyethyl)piperidine

: 460997-30-2
2-[2-(1-benzyl-6-oxo-1,4,5,6-tetrahydro-pyridin-3-yl)-2-hydroxy-ethyl]-piperidine-1-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 7 steps

1.1: 65 percent / CrO₃; H₂SO₄

2.1: 86 percent / NaOH / 2-methyl-propan-2-ol

3.1: 71 percent / DCC; DMPA / tetrahydrofuran / 17 h / 20 °C

4.1: tetrahydrofuran / 0.5 h / -78 °C

4.2: tetrahydrofuran; methanol / -50 - -5 °C

5.1: 84 percent / TBAF / tetrahydrofuran; methanol / 0.5 h / -20 °C

6.1: tetrahydrofuran / 18 h / 20 °C

6.2: 56 percent / tetrahydrofuran / 18 h / Heating

7.1: NaBH₄ / tetrahydrofuran; methanol / 2 h / 0 °C

With chromium(VI) oxide; sodium hydroxide; sodium tetrahydroborate; sulfuric acid; 0,2,4-dichlorophenyl-0-methylisopropylamidothiophosphate; tetrabutyl ammonium fluoride; dicyclohexyl-carbodiimide; In tetrahydrofuran; methanol; tert-butyl alcohol;
DOI:10.1021/ol0263144

Reference yield:

: 19832-04-3
2-(piperidin-2-yl)acetic acid

: 460997-30-2
2-[2-(1-benzyl-6-oxo-1,4,5,6-tetrahydro-pyridin-3-yl)-2-hydroxy-ethyl]-piperidine-1-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 6 steps

1.1: 86 percent / NaOH / 2-methyl-propan-2-ol

2.1: 71 percent / DCC; DMPA / tetrahydrofuran / 17 h / 20 °C

3.1: tetrahydrofuran / 0.5 h / -78 °C

3.2: tetrahydrofuran; methanol / -50 - -5 °C

4.1: 84 percent / TBAF / tetrahydrofuran; methanol / 0.5 h / -20 °C

5.1: tetrahydrofuran / 18 h / 20 °C

5.2: 56 percent / tetrahydrofuran / 18 h / Heating

6.1: NaBH₄ / tetrahydrofuran; methanol / 2 h / 0 °C

With sodium hydroxide; sodium tetrahydroborate; 0,2,4-dichlorophenyl-0-methylisopropylamidothiophosphate; tetrabutyl ammonium fluoride; dicyclohexyl-carbodiimide; In tetrahydrofuran; methanol; tert-butyl alcohol;
DOI:10.1021/ol0263144