methyl 3-methyl-4-(1-methyl-7-oxo-3-(pyridin-2-yl)-1,4,5,6,7,8-hexahydrocyclohepta[c]pyrazol-4-yl)benzoate

Base Information

Chemical Name:methyl 3-methyl-4-(1-methyl-7-oxo-3-(pyridin-2-yl)-1,4,5,6,7,8-hexahydrocyclohepta[c]pyrazol-4-yl)benzoate
CAS No.:1616364-27-2
Molecular Formula:C₂₃H₂₃N₃O₃
Molecular Weight:389.454
Hs Code.:

Synonyms:methyl 3-methyl-4-(1-methyl-7-oxo-3-(pyridin-2-yl)-1,4,5,6,7,8-hexahydrocyclohepta[c]pyrazol-4-yl)benzoate

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Chemical Property of methyl 3-methyl-4-(1-methyl-7-oxo-3-(pyridin-2-yl)-1,4,5,6,7,8-hexahydrocyclohepta[c]pyrazol-4-yl)benzoate

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Technology Process of methyl 3-methyl-4-(1-methyl-7-oxo-3-(pyridin-2-yl)-1,4,5,6,7,8-hexahydrocyclohepta[c]pyrazol-4-yl)benzoate

There total 4 articles about methyl 3-methyl-4-(1-methyl-7-oxo-3-(pyridin-2-yl)-1,4,5,6,7,8-hexahydrocyclohepta[c]pyrazol-4-yl)benzoate 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: 88.0%

: 70-25-7
N-Methyl-N'-nitro-N-nitrosoguanidine

: 1616364-26-1
3-methyl-4-(1-methyl-7-oxo-3-(pyridin-2-yl)-1,4,5,6,7,8-hexahydrocyclohepta[c]pyrazol-4-yl)benzoic acid

: 1616364-27-2
methyl 3-methyl-4-(1-methyl-7-oxo-3-(pyridin-2-yl)-1,4,5,6,7,8-hexahydrocyclohepta[c]pyrazol-4-yl)benzoate

Guidance literature:: With potassium hydroxide; In tetrahydrofuran; diethyl ether; water; at 0 ℃; Inert atmosphere;

Reference yield:

: 1616364-24-9
methyl 4-(1-(5-chloro-1-methyl-3-(pyridin-2-yl)-1H-pyrazol-4-yl)-4-methoxy-4-oxobutyl)-3-methylbenzoate

: 1616364-27-2
methyl 3-methyl-4-(1-methyl-7-oxo-3-(pyridin-2-yl)-1,4,5,6,7,8-hexahydrocyclohepta[c]pyrazol-4-yl)benzoate

Guidance literature:: Multi-step reaction with 3 steps

1.1: XPhos; dmap; bis(η3-allyl-μ-chloropalladium(II)) / 1,3,5-trimethyl-benzene / 16 h / 120 °C / Inert atmosphere

2.1: toluene / 16 h / Molecular sieve; Reflux

2.2: 22 h / 0 - 20 °C

3.1: potassium hydroxide / diethyl ether; tetrahydrofuran; water / 0 °C / Inert atmosphere

With dmap; bis(η3-allyl-μ-chloropalladium(II)); potassium hydroxide; XPhos; In tetrahydrofuran; diethyl ether; water; toluene; 1,3,5-trimethyl-benzene;

Reference yield:

: 1616364-25-0
methyl 4-(1-(5-(2-ethoxy-2-oxoethyl)-1-methyl-3-(pyridin-2-yl)-1H-pyrazol-4-yl)-4-methoxy-4-oxobutyl)-3-methylbenzoate

: 1616364-27-2
methyl 3-methyl-4-(1-methyl-7-oxo-3-(pyridin-2-yl)-1,4,5,6,7,8-hexahydrocyclohepta[c]pyrazol-4-yl)benzoate

Guidance literature:: Multi-step reaction with 2 steps

1.1: toluene / 16 h / Molecular sieve; Reflux

1.2: 22 h / 0 - 20 °C

2.1: potassium hydroxide / diethyl ether; tetrahydrofuran; water / 0 °C / Inert atmosphere

With potassium hydroxide; In tetrahydrofuran; diethyl ether; water; toluene;