Pyrrolo[1,2-a]quinazolin-5(1H)-one, 2,3-dihydro-

Base Information

Chemical Name:Pyrrolo[1,2-a]quinazolin-5(1H)-one, 2,3-dihydro-
CAS No.:16198-97-3
Molecular Formula:C11H10N2O
Molecular Weight:186.213
Hs Code.:
DSSTox Substance ID:DTXSID60484120
Nikkaji Number:J1.866.601D
Wikidata:Q82322179
Mol file:16198-97-3.mol

Synonyms:16198-97-3;Pyrrolo[1,2-a]quinazolin-5(1H)-one, 2,3-dihydro-;SCHEMBL20704914;DTXSID60484120;1,2-trimethylene-1,4-dihydro-4-quinazolone;2,3-dihydropyrrolo[1,2-a]quinazolin-5(1H)-one;1,2,3,10-tetrahydro-pyrrolo[1,2-a]quinazolin-5-one

Suppliers and Price of Pyrrolo[1,2-a]quinazolin-5(1H)-one, 2,3-dihydro-

Supply Marketing:

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

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Chemical Property of Pyrrolo[1,2-a]quinazolin-5(1H)-one, 2,3-dihydro-

Chemical Property:

XLogP3:0.9
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:0
Exact Mass:186.079312947
Heavy Atom Count:14
Complexity:298

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CC2=NC(=O)C3=CC=CC=C3N2C1

Technology Process of Pyrrolo[1,2-a]quinazolin-5(1H)-one, 2,3-dihydro-

There total 1 articles about Pyrrolo[1,2-a]quinazolin-5(1H)-one, 2,3-dihydro- 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: 77.0%

: 22458-07-7
N-(2-benzamido)-4-chlorobutanamide

: 530-53-0
deoxyvasicinone

: 16198-97-3
2,3-dihydropyrrolo<1,2-a>quinazolin-5(1H)-one

Guidance literature:: With potassium tert-butylate; In tetrahydrofuran; at 20 ℃; for 0.25h; Reagent/catalyst; Inert atmosphere;
DOI:10.1055/s-0035-1562792

Reference yield: 99.26%

: 1665-94-7
N-(4-formylphenyl)-4-methylbenzenesulfonamide

: 16198-97-3
2,3-dihydropyrrolo<1,2-a>quinazolin-5(1H)-one

: (E)-4-methyl-N-(4-((5-oxo-1,2-dihydropyrrolo[1,2-a]quinazolin-3(5H)-ylidene)methyl)phenyl)benzenesulfonamide

Guidance literature:: With sodium methylate; In methanol; at 0 - 90 ℃; for 2h;

Reference yield: 95.0%

: 100-52-7
benzaldehyde

: 16198-97-3
2,3-dihydropyrrolo<1,2-a>quinazolin-5(1H)-one

: 107954-53-0
2,3-dihydro-3-(phenylmethylene)pyrrolo<2,1-b>quinazolin-5(1H)-one

Guidance literature:: With sodium acetate; In acetic acid; at 110 ℃; for 4h; stereoselective reaction; Inert atmosphere;
DOI:10.1055/s-0035-1562792