Catalog No.:AA00C7ZJ

32092-18-5 | Ethyl 4-oxo-4H-pyrido[1,2-a]pyrimidine-3-carboxylate

Name: Name:Ethyl 4-oxo-4H-pyrido[1,2-a]pyrimidine-3-carboxylate
Brand: AABLOCKS
SKU: AA00C7ZJ
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Technical Information
Properties
Downstream Synthesis Route
Literature
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Technical Information
Properties
Downstream Synthesis Route
Literature

Technical Information

Catalog Number:

AA00C7ZJ

Chemical Name:

Ethyl 4-oxo-4H-pyrido[1,2-a]pyrimidine-3-carboxylate

CAS Number:

32092-18-5

Molecular Formula:

C11H10N2O3

Molecular Weight:

218.2087

MDL Number:

MFCD02102304

SMILES:

CCOC(=O)c1cnc2n(c1=O)cccc2

NSC Number:

518312

Properties

Form:

Solid

MP:

110-111℃

Storage:

Keep in dry area;2-8℃;

Computed Properties

Complexity:

458

Covalently-Bonded Unit Count:

Heavy Atom Count:

Hydrogen Bond Acceptor Count:

Rotatable Bond Count:

XLogP3:

0.2

Downstream Synthesis Route

32092-18-5

34662-58-3

[1]Mane;Li;Huang;Gupta;Nadkarni;Giridhar;Naik;Yadav[BioorganicandMedicinalChemistry,2012,vol.20,#21,p.6296-6304]

[2]Adams;Pachter[JournaloftheAmericanChemicalSociety,1952,vol.74,p.5491,5495][JournaloftheAmericanChemicalSociety,1953,vol.75,p.6357]

[3]CurrentPatentAssignee:GLAXOSMITHKLINEPLC-US4081545,1978,A

[4]CurrentPatentAssignee:HUTCHISONCHINAMEDITECHLTD.-WO2021/197276,2021,A1Locationinpatent:Page/Pagecolumn53

32092-18-5

39080-62-1

[1]Adams;Pachter[JournaloftheAmericanChemicalSociety,1952,vol.74,p.5491,5495][JournaloftheAmericanChemicalSociety,1953,vol.75,p.6357]

39080-52-9

32092-18-5

[1]Hajimahdi;Zarghi;Zabihollahi;Aghasadeghi[MedicinalChemistryResearch,2013,vol.22,#5,p.2467-2475]

[2]Mane;Li;Huang;Gupta;Nadkarni;Giridhar;Naik;Yadav[BioorganicandMedicinalChemistry,2012,vol.20,#21,p.6296-6304]

[3]CurrentPatentAssignee:GANJIANGNEWDISTRBRIGHTGENEINNOVATIVEMEDICINE;GANNJIANGNEWDISTRBOELEINNOVATIVEMEDICINE-WO2022/89389,2022,A1Locationinpatent:Page/Pagecolumn16-17

[4]CurrentPatentAssignee:RYVUTHERAPEUTICSSA-WO2019/238786,2019,A1Locationinpatent:Page/Pagecolumn75;74

[5]Locationinpatent:schemeortableLengyel,László;Nagy,TiborZs.;Sipos,Gellért;Jones,Richard;Dormán,György;Ürge,László;Darvas,Ferenc[TetrahedronLetters,2012,vol.53,#7,p.738-743]

[6]Adams;Pachter[JournaloftheAmericanChemicalSociety,1952,vol.74,p.5491,5495][JournaloftheAmericanChemicalSociety,1953,vol.75,p.6357]

[7]Hermecz,Istvan;Horvath,Agnes;Vasvari-Debreczy,Lelle;Meszaros,Zoltan[Synthesis,1984,#2,p.152-158]

[8]Prager,RolfH.;Singh,Yogendra[AustralianJournalofChemistry,1994,vol.47,#7,p.1263-1270]

[9]Boese,A.Daniel;Dallinger,Doris;Darvas,Ferenc;Hartmann,PeterE.;Kappe,C.Oliver;Sipos,Gellért;Wernik,Michaela[EuropeanJournalofOrganicChemistry,2020,vol.2020,#45,p.7051-7061]

32092-18-5

38326-36-2

[1]Podanyi,Benjamin;Hermecz,Istvan;Vasvari-Debreczy,Lelle;Horvath,Agnes[JournalofOrganicChemistry,1986,vol.51,#3,p.394-399]

[2]CurrentPatentAssignee:GANJIANGNEWDISTRBRIGHTGENEINNOVATIVEMEDICINE;GANNJIANGNEWDISTRBOELEINNOVATIVEMEDICINE-WO2022/89389,2022,A1Locationinpatent:Page/Pagecolumn16-17

Literature

Title: Synthesis and SAR studies of 1,4-benzoxazine MenB inhibitors: novel antibacterial agents against Mycobacterium tuberculosis.

Journal: Bioorganic & medicinal chemistry letters 20101101

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