1-{1-[(benzyloxy)carbonyl]piperidin-4-yl}-2-oxoindoline-5-carboxylic acid

Base Information

Chemical Name:1-{1-[(benzyloxy)carbonyl]piperidin-4-yl}-2-oxoindoline-5-carboxylic acid
CAS No.:1037834-35-7
Molecular Formula:C₂₂H₂₂N₂O₅
Molecular Weight:394.427
Hs Code.:

Synonyms:1-{1-[(benzyloxy)carbonyl]piperidin-4-yl}-2-oxoindoline-5-carboxylic acid

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Chemical Property of 1-{1-[(benzyloxy)carbonyl]piperidin-4-yl}-2-oxoindoline-5-carboxylic acid

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Technology Process of 1-{1-[(benzyloxy)carbonyl]piperidin-4-yl}-2-oxoindoline-5-carboxylic acid

There total 10 articles about 1-{1-[(benzyloxy)carbonyl]piperidin-4-yl}-2-oxoindoline-5-carboxylic acid 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: 97.0%

: 1037834-34-6
methyl 1-(1-(benzyloxycarbonyl)-piperidin-4-yl)-2-oxoindoline-5-carboxylate

: 1037834-35-7
1-{1-[(benzyloxy)carbonyl]piperidin-4-yl}-2-oxoindoline-5-carboxylic acid

Guidance literature:: methyl 1-(1-(benzyloxycarbonyl)-piperidin-4-yl)-2-oxoindoline-5-carboxylate; With methanol; sodium hydroxide; water; at 80 ℃; for 2h;

With hydrogenchloride; water; In methanol; at 20 ℃;

Product distribution / selectivity;

Reference yield:

: 19099-93-5
benzyl 4-oxo-1-piperidinecarboxylate

: 1037834-35-7
1-{1-[(benzyloxy)carbonyl]piperidin-4-yl}-2-oxoindoline-5-carboxylic acid

Guidance literature:: Multi-step reaction with 4 steps

1.1: sodium tris(acetoxy)borohydride; acetic acid / dichloromethane / 6 h / 20 °C

1.2: 1 h

2.1: pyridine / ethyl acetate / 1 h / 20 °C

3.1: triethylamine / palladium diacetate; johnphos / 2-methyltetrahydrofuran; isopropyl alcohol / 2 h / 80 °C

4.1: methanol; sodium hydroxide; water / acetonitrile / 2 h / 60 - 72 °C

4.2: 1 h / 20 - 50 °C

With pyridine; methanol; sodium hydroxide; water; sodium tris(acetoxy)borohydride; acetic acid; triethylamine; palladium diacetate; johnphos; In 2-methyltetrahydrofuran; dichloromethane; ethyl acetate; isopropyl alcohol; acetonitrile;

Reference yield:

: 196103-67-0
di-tert-butyl [5-(methoxycarbonyl)-2-nitrophenyl]malonate

: 1037834-35-7
1-{1-[(benzyloxy)carbonyl]piperidin-4-yl}-2-oxoindoline-5-carboxylic acid

Guidance literature:: Multi-step reaction with 4 steps

1.1: nickel / methanol

2.1: sodium tris(acetoxy)borohydride; acetic acid / 1,2-dichloro-ethane / 76 h / 20 °C

3.1: toluene-4-sulfonic acid / toluene / 2 h / Heating / reflux

4.1: methanol; sodium hydroxide; water / acetonitrile / 2 h / 60 - 72 °C

4.2: 1 h / 20 - 50 °C

With methanol; sodium hydroxide; water; sodium tris(acetoxy)borohydride; toluene-4-sulfonic acid; acetic acid; nickel; In methanol; 1,2-dichloro-ethane; toluene; acetonitrile;