4(1H)-Pyrimidinone, 2-((2-(((5-methyl-1H-imidazol-4-yl)methyl)thio)ethyl)amino)-5-(2-thiazolylmethyl)-, trihydrochloride

Base Information

Chemical Name:4(1H)-Pyrimidinone, 2-((2-(((5-methyl-1H-imidazol-4-yl)methyl)thio)ethyl)amino)-5-(2-thiazolylmethyl)-, trihydrochloride
CAS No.:64107-58-0
Molecular Formula:C₁₅H₁₈N₆OS₂*3ClH
Molecular Weight:471.862
Hs Code.:
DSSTox Substance ID:DTXSID30214315

Synonyms:4(1H)-Pyrimidinone, 2-((2-(((5-methyl-1H-imidazol-4-yl)methyl)thio)ethyl)amino)-5-(2-thiazolylmethyl)-, trihydrochloride;64107-58-0;C15H18N6OS2.3ClH;DTXSID30214315;C15-H18-N6-O-S2.3Cl-H;LS-135977

Suppliers and Price of 4(1H)-Pyrimidinone, 2-((2-(((5-methyl-1H-imidazol-4-yl)methyl)thio)ethyl)amino)-5-(2-thiazolylmethyl)-, trihydrochloride

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 1 raw suppliers

Chemical Property of 4(1H)-Pyrimidinone, 2-((2-(((5-methyl-1H-imidazol-4-yl)methyl)thio)ethyl)amino)-5-(2-thiazolylmethyl)-, trihydrochloride

Chemical Property:

Vapor Pressure:1.97E-18mmHg at 25°C
Boiling Point:674.5°Cat760mmHg
Flash Point:361.7°C
Density:g/cm³
Hydrogen Bond Donor Count:6
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:8
Exact Mass:470.028385
Heavy Atom Count:27
Complexity:512

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=C(N=CN1)CSCCNC2=NC=C(C(=O)N2)CC3=NC=CS3.Cl.Cl.Cl

Technology Process of 4(1H)-Pyrimidinone, 2-((2-(((5-methyl-1H-imidazol-4-yl)methyl)thio)ethyl)amino)-5-(2-thiazolylmethyl)-, trihydrochloride

There total 6 articles about 4(1H)-Pyrimidinone, 2-((2-(((5-methyl-1H-imidazol-4-yl)methyl)thio)ethyl)amino)-5-(2-thiazolylmethyl)-, trihydrochloride 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: 34.0%

: 38585-67-0
4-{[(2-aminoethyl)thio]methyl}-5-methylimidazole

: 64107-62-6
5-<2>Thiazolylmethyl-2-methylthio-4-pyrimidon

: 64107-58-0
2-[2-(5-Methyl-1H-imidazol-4-ylmethylsulfanyl)-ethylamino]-5-thiazol-2-ylmethyl-1H-pyrimidin-4-one; hydrochloride

Guidance literature:: With hydrogenchloride; at 145 - 150 ℃; for 5h;
DOI:10.1016/0223-5234(89)90166-9

Reference yield:

: 52396-77-7
3-thiazol-2-yl-acrylic acid

: 64107-58-0
2-[2-(5-Methyl-1H-imidazol-4-ylmethylsulfanyl)-ethylamino]-5-thiazol-2-ylmethyl-1H-pyrimidin-4-one; hydrochloride

Guidance literature:: Multi-step reaction with 6 steps

1: conc. H₂SO₄

2: H₂ / 5percent Pd/C / ethanol / 45 °C

3: sodium wire / diethyl ether / 18 h / Ambient temperature

4: ethanol / 7 h / Heating

5: 77 percent / NaOH / H₂O; ethanol / 60 °C

6: 34 percent / 2.) ethanolic hydrogen chloride / 5 h / 145 - 150 °C

With hydrogenchloride; sodium hydroxide; sulfuric acid; hydrogen; sodium; palladium on activated charcoal; In diethyl ether; ethanol; water;
DOI:10.1016/0223-5234(89)90166-9

Reference yield:

: 64107-59-1
(E)-3-Thiazol-2-yl-acrylic acid ethyl ester

: 64107-58-0
2-[2-(5-Methyl-1H-imidazol-4-ylmethylsulfanyl)-ethylamino]-5-thiazol-2-ylmethyl-1H-pyrimidin-4-one; hydrochloride

Guidance literature:: Multi-step reaction with 5 steps

1: H₂ / 5percent Pd/C / ethanol / 45 °C

2: sodium wire / diethyl ether / 18 h / Ambient temperature

3: ethanol / 7 h / Heating

4: 77 percent / NaOH / H₂O; ethanol / 60 °C

5: 34 percent / 2.) ethanolic hydrogen chloride / 5 h / 145 - 150 °C

With hydrogenchloride; sodium hydroxide; hydrogen; sodium; palladium on activated charcoal; In diethyl ether; ethanol; water;
DOI:10.1016/0223-5234(89)90166-9