2-(2-Methoxy-4-methylsulfinylphenyl)imidazo[1,2-a]pyrimidine

Base Information

Chemical Name:2-(2-Methoxy-4-methylsulfinylphenyl)imidazo[1,2-a]pyrimidine
CAS No.:93276-61-0
Molecular Formula:C₁₄H₁₃N₃O₂S
Molecular Weight:287.342
Hs Code.:
ChEMBL ID:CHEMBL147753
DSSTox Substance ID:DTXSID80874509
Nikkaji Number:J489.846J

Synonyms:93276-61-0;CHEMBL147753;SCHEMBL10793366;DTXSID80874509;IMIDAZO[1,2-A]PYRIMIDINE, 2-[2-METHOXY-4-(METHYL

Suppliers and Price of 2-(2-Methoxy-4-methylsulfinylphenyl)imidazo[1,2-a]pyrimidine

Supply Marketing:

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

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Chemical Property of 2-(2-Methoxy-4-methylsulfinylphenyl)imidazo[1,2-a]pyrimidine

Chemical Property:

XLogP3:1.9
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:3
Exact Mass:287.07284784
Heavy Atom Count:20
Complexity:368

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:COC1=C(C=CC(=C1)S(=O)C)C2=CN3C=CC=NC3=N2

Technology Process of 2-(2-Methoxy-4-methylsulfinylphenyl)imidazo[1,2-a]pyrimidine

There total 7 articles about 2-(2-Methoxy-4-methylsulfinylphenyl)imidazo[1,2-a]pyrimidine 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: 36.0%

: 109-12-6
2-aminopyrimidine

: 93276-67-6
2-bromo-2'-methoxy-4'-methylsulphinylacetophenone

: 93276-61-0
2-(2-methoxy-4-methylsulphinylphenyl)imidazo<1,2-a>pyrimidine

Guidance literature:: In ethanol; at 80 ℃; for 5h;
DOI:10.1016/0223-5234(92)90004-K

Reference yield:

: 72856-73-6
2-methoxy-4-(methylsulfanyl)benzoic acid

: 93276-61-0
2-(2-methoxy-4-methylsulphinylphenyl)imidazo<1,2-a>pyrimidine

Guidance literature:: Multi-step reaction with 6 steps

1: SOCl₂ / 1 h / Heating

2: 1.) n-BuLi / 1.) ether, hexane, -60 deg C, 2.) ether, hexane, THF, a) 0-5 deg C, 1 h, b) RT, 2 h

3: dioxane / 0.5 h / Heating

4: 65 percent / CuBr₂ / CHCl₃; ethyl acetate / 3 h / Heating

5: 60 percent / m-chloroperbenzoic acid / CHCl₃ / 3 h / 0 °C

6: 36 percent / ethanol / 5 h / 80 °C

With n-butyllithium; thionyl chloride; 3-chloro-benzenecarboperoxoic acid; copper(ll) bromide; In 1,4-dioxane; ethanol; chloroform; ethyl acetate;
DOI:10.1016/0223-5234(92)90004-K

Reference yield:

: 69883-78-9
2-methoxy-4-(methylthio)benzoyl chloride

: 93276-61-0
2-(2-methoxy-4-methylsulphinylphenyl)imidazo<1,2-a>pyrimidine

Guidance literature:: Multi-step reaction with 5 steps

1: 1.) n-BuLi / 1.) ether, hexane, -60 deg C, 2.) ether, hexane, THF, a) 0-5 deg C, 1 h, b) RT, 2 h

2: dioxane / 0.5 h / Heating

3: 65 percent / CuBr₂ / CHCl₃; ethyl acetate / 3 h / Heating

4: 60 percent / m-chloroperbenzoic acid / CHCl₃ / 3 h / 0 °C

5: 36 percent / ethanol / 5 h / 80 °C

With n-butyllithium; 3-chloro-benzenecarboperoxoic acid; copper(ll) bromide; In 1,4-dioxane; ethanol; chloroform; ethyl acetate;
DOI:10.1016/0223-5234(92)90004-K