Ethyl 7-(4-chlorobenzoyl)-3-(2-fluorophenyl)pyrrolo[1,2-c]pyrimidine-5-carboxylate

Base Information

Chemical Name:Ethyl 7-(4-chlorobenzoyl)-3-(2-fluorophenyl)pyrrolo[1,2-c]pyrimidine-5-carboxylate
CAS No.:302912-52-3
Molecular Formula:C₂₃H₁₆ClFN₂O₃
Molecular Weight:422.843
Hs Code.:
European Community (EC) Number:658-778-8

Synonyms:ethyl 7-(4-chlorobenzoyl)-3-(2-fluorophenyl)pyrrolo[1,2-c]pyrimidine-5-carboxylate;302912-52-3;AKOS024327056

Suppliers and Price of Ethyl 7-(4-chlorobenzoyl)-3-(2-fluorophenyl)pyrrolo[1,2-c]pyrimidine-5-carboxylate

Supply Marketing:

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

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Chemical Property of Ethyl 7-(4-chlorobenzoyl)-3-(2-fluorophenyl)pyrrolo[1,2-c]pyrimidine-5-carboxylate

Chemical Property:

XLogP3:6.1
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:6
Exact Mass:422.0833482
Heavy Atom Count:30
Complexity:628

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCOC(=O)C1=C2C=C(N=CN2C(=C1)C(=O)C3=CC=C(C=C3)Cl)C4=CC=CC=C4F

Technology Process of Ethyl 7-(4-chlorobenzoyl)-3-(2-fluorophenyl)pyrrolo[1,2-c]pyrimidine-5-carboxylate

There total 2 articles about Ethyl 7-(4-chlorobenzoyl)-3-(2-fluorophenyl)pyrrolo[1,2-c]pyrimidine-5-carboxylate 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: 46.0%

: 1235649-95-2
4-(2-fluorophenyl)pyrimidine

: 536-38-9
4-chlorobenzoylmethyl bromide

: 623-47-2
propynoic acid ethyl ester

: 302912-52-3
C₂₃H₁₆ClFN₂O₃

Guidance literature:: With ethyloxirane; at 120 ℃; for 0.5h; Sealed tube; Microwave irradiation; Green chemistry;
DOI:10.2174/13862073113169990050

Reference yield:

: 445-27-2
2'-Fluoroacetophenone

: 302912-52-3
C₂₃H₁₆ClFN₂O₃

Guidance literature:: Multi-step reaction with 2 steps

1: toluene-4-sulfonic acid

2: ethyloxirane / 0.5 h / 120 °C / Sealed tube; Microwave irradiation; Green chemistry

With ethyloxirane; toluene-4-sulfonic acid;
DOI:10.2174/13862073113169990050