1-fenil-3-metil-4-carbetossi-5-cloroacetammidopirazolo-O-metil derivato

Base Information

Chemical Name:1-fenil-3-metil-4-carbetossi-5-cloroacetammidopirazolo-O-metil derivato
CAS No.:126567-96-2
Molecular Formula:C₁₆H₁₈ClN₃O₃
Molecular Weight:335.79
Hs Code.:

Synonyms:1-fenil-3-metil-4-carbetossi-5-cloroacetammidopirazolo-O-metil derivato

Suppliers and Price of 1-fenil-3-metil-4-carbetossi-5-cloroacetammidopirazolo-O-metil derivato

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 1-fenil-3-metil-4-carbetossi-5-cloroacetammidopirazolo-O-metil derivato

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Technology Process of 1-fenil-3-metil-4-carbetossi-5-cloroacetammidopirazolo-O-metil derivato

There total 2 articles about 1-fenil-3-metil-4-carbetossi-5-cloroacetammidopirazolo-O-metil derivato 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: 45.0%

: 186581-53-3,908094-01-9,334-88-3
diazomethane

: 126567-94-0
1-fenil-3-metil-4-carbetossi-5-cloroacetammidopirazolo

: 126567-96-2
1-fenil-3-metil-4-carbetossi-5-cloroacetammidopirazolo-O-metil derivato

: 126567-95-1
N-metil-N-(1-fenil-3-metil-4-carbetossi-pirazol-5-yl)cloroacetammide

Guidance literature:: In diethyl ether; for 24h;

Reference yield:

: 121716-27-6
5-amino-3-methyl-1-phenyl-1H-pyrazole-4-carboxylic acid ethyl ester

: 126567-96-2
1-fenil-3-metil-4-carbetossi-5-cloroacetammidopirazolo-O-metil derivato

Guidance literature:: Multi-step reaction with 2 steps

1: 60 percent / toluene / 20 h / Heating

2: 30 percent / diethyl ether / 24 h

In diethyl ether; toluene;

Reference yield:

: 126567-96-2
1-fenil-3-metil-4-carbetossi-5-cloroacetammidopirazolo-O-metil derivato

: 1131-18-6
1-Phenyl-3-methyl-5-aminopyrazole

Guidance literature:: With potassium hydroxide; Yield given. Multistep reaction; 1.) H₂O, EtOH, reflux, 10 h; 2.) neat (solid), 200 deg C, 15 min;