(3R,4R)-4-[4-[3-(2-methoxy-benzyloxy)-propoxy]-phenyl]-3-(quinolin-7-yl-methoxy)-piperidine-1-carboxylic acid tert-butyl ester

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Chemical Name:(3R,4R)-4-[4-[3-(2-methoxy-benzyloxy)-propoxy]-phenyl]-3-(quinolin-7-yl-methoxy)-piperidine-1-carboxylic acid tert-butyl ester
CAS No.:257938-72-0
Molecular Formula:C₃₇H₄₄N₂O₆
Molecular Weight:612.766
Hs Code.:

Synonyms:(3R,4R)-4-[4-[3-(2-methoxy-benzyloxy)-propoxy]-phenyl]-3-(quinolin-7-yl-methoxy)-piperidine-1-carboxylic acid tert-butyl ester

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Chemical Property of (3R,4R)-4-[4-[3-(2-methoxy-benzyloxy)-propoxy]-phenyl]-3-(quinolin-7-yl-methoxy)-piperidine-1-carboxylic acid tert-butyl ester

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Technology Process of (3R,4R)-4-[4-[3-(2-methoxy-benzyloxy)-propoxy]-phenyl]-3-(quinolin-7-yl-methoxy)-piperidine-1-carboxylic acid tert-butyl ester

There total 8 articles about (3R,4R)-4-[4-[3-(2-methoxy-benzyloxy)-propoxy]-phenyl]-3-(quinolin-7-yl-methoxy)-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: 94.0%

: 188874-61-5
7-bromomethyl-quinoline hydrobromide

: 257938-68-4
(3R,4R)-3-hydroxy-4-[4-[3-(2-methoxy-benzyloxy)-propoxy]-phenyl]-piperidine-1-carboxylic acid tert-butyl ester

: 257938-72-0
(3R,4R)-4-[4-[3-(2-methoxy-benzyloxy)-propoxy]-phenyl]-3-(quinolin-7-yl-methoxy)-piperidine-1-carboxylic acid tert-butyl ester

Guidance literature:: With sodium hydride; In N,N-dimethyl-formamide; at 20 ℃; for 24h;
DOI:10.1016/S0014-827X(01)01004-7

Reference yield:

: 257928-43-1
(R)-4-(4-benzyloxy-phenyl)-1-(1-phenyl-ethyl)-1,2,3,6-tetrahydro-pyridine

: 257938-72-0
(3R,4R)-4-[4-[3-(2-methoxy-benzyloxy)-propoxy]-phenyl]-3-(quinolin-7-yl-methoxy)-piperidine-1-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 5 steps

1.1: BH₃*THF / tetrahydrofuran / 1 h / 20 °C

1.2: 50 percent / aq. NaOH; H₂O₂ / tetrahydrofuran / 3 h / 45 °C

2.1: H₂ / Pd/C / methanol / 15 h / 20 °C

3.1: Et₃N / methanol / 3 h / -10 - 0 °C

4.1: 88 percent / K₂CO₃ / dimethylformamide / 66 h / 120 °C

5.1: 94 percent / NaH / dimethylformamide / 24 h / 20 °C

With borane-THF; hydrogen; sodium hydride; potassium carbonate; triethylamine; palladium on activated charcoal; In tetrahydrofuran; methanol; N,N-dimethyl-formamide;
DOI:10.1016/S0014-827X(01)01004-7

Reference yield:

: 257938-64-0
(3R,4R)-4-(4-benzyloxy-phenyl)-1-((R)-1-phenyl-ethyl)-piperidin-3-ol

: 257938-72-0
(3R,4R)-4-[4-[3-(2-methoxy-benzyloxy)-propoxy]-phenyl]-3-(quinolin-7-yl-methoxy)-piperidine-1-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: H₂ / Pd/C / methanol / 15 h / 20 °C

2: Et₃N / methanol / 3 h / -10 - 0 °C

3: 88 percent / K₂CO₃ / dimethylformamide / 66 h / 120 °C

4: 94 percent / NaH / dimethylformamide / 24 h / 20 °C

With hydrogen; sodium hydride; potassium carbonate; triethylamine; palladium on activated charcoal; In methanol; N,N-dimethyl-formamide;
DOI:10.1016/S0014-827X(01)01004-7