5-(1-(tert-butoxycarbonyl)piperidin-4-yl)-1-(4-isopropylphenyl)-1H-pyrazole-4-carboxylic acid

Base Information

Chemical Name:5-(1-(tert-butoxycarbonyl)piperidin-4-yl)-1-(4-isopropylphenyl)-1H-pyrazole-4-carboxylic acid
CAS No.:1020050-02-5
Molecular Formula:C₂₃H₃₁N₃O₄
Molecular Weight:413.517
Hs Code.:

Synonyms:5-(1-(tert-butoxycarbonyl)piperidin-4-yl)-1-(4-isopropylphenyl)-1H-pyrazole-4-carboxylic acid

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Chemical Property of 5-(1-(tert-butoxycarbonyl)piperidin-4-yl)-1-(4-isopropylphenyl)-1H-pyrazole-4-carboxylic acid

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Technology Process of 5-(1-(tert-butoxycarbonyl)piperidin-4-yl)-1-(4-isopropylphenyl)-1H-pyrazole-4-carboxylic acid

There total 8 articles about 5-(1-(tert-butoxycarbonyl)piperidin-4-yl)-1-(4-isopropylphenyl)-1H-pyrazole-4-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: 68.0%

: 957247-54-0
tert-butyl 4-(4-(ethoxycarbonyl)-1-(4-isopropylphenyl)-1H-pyrazol-5-yl)piperidine-1-carboxylate

: 1020050-02-5
5-(1-(tert-butoxycarbonyl)piperidin-4-yl)-1-(4-isopropylphenyl)-1H-pyrazole-4-carboxylic acid

Guidance literature:: tert-butyl 4-(4-(ethoxycarbonyl)-1-(4-isopropylphenyl)-1H-pyrazol-5-yl)piperidine-1-carboxylate; With sodium hydroxide; In ethanol; water; at 70 ℃; for 20h;

With hydrogenchloride; In water; at 0 ℃; pH=2;
DOI:10.1021/jm200782y

Reference yield:

: 1336874-05-5
(E,Z)-tert-butyl-4-(3-ethoxy-2-(ethoxycarbonyl)acryloyl)piperidine-1-carboxylate

: 1020050-02-5
5-(1-(tert-butoxycarbonyl)piperidin-4-yl)-1-(4-isopropylphenyl)-1H-pyrazole-4-carboxylic acid

Guidance literature:: Multi-step reaction with 2 steps

1.1: sodium hydrogencarbonate / dichloromethane

1.2: 48 h / 100 °C / Reflux

2.1: sodium hydroxide / ethanol; water / 20 h / 70 °C

2.2: 0 °C / pH 2

With sodium hydrogencarbonate; sodium hydroxide; In ethanol; dichloromethane; water;
DOI:10.1021/jm200782y

Reference yield:

: 1336874-02-2
tert‐butyl 4‐(2,2‐dimethyl‐4,6‐dioxo‐1,3‐dioxane‐5‐carbonyl)piperidine‐1‐carboxylate

: 1020050-02-5
5-(1-(tert-butoxycarbonyl)piperidin-4-yl)-1-(4-isopropylphenyl)-1H-pyrazole-4-carboxylic acid

Guidance literature:: Multi-step reaction with 4 steps

1.1: 48 h / Reflux

2.1: acetic anhydride / 48 h / 100 °C / Inert atmosphere

3.1: sodium hydrogencarbonate / dichloromethane

3.2: 48 h / 100 °C / Reflux

4.1: sodium hydroxide / ethanol; water / 20 h / 70 °C

4.2: 0 °C / pH 2

With acetic anhydride; sodium hydrogencarbonate; sodium hydroxide; In ethanol; dichloromethane; water;
DOI:10.1021/jm200782y