1-Benzyl-1H-pyrido[2,3-d][1,3]oxazine-2,4-dione

Base Information

• Chemical Name: 1-Benzyl-1H-pyrido[2,3-d][1,3]oxazine-2,4-dione
• CAS No.: 97484-73-6
• Molecular Formula: C14H10N2O3
• Molecular Weight: 254.245
• Hs Code.: 2934999090
• DSSTox Substance ID: DTXSID60540437
• Wikidata: Q82416453
• Mol file: 97484-73-6.mol

Synonyms:1-Benzyl-1H-pyrido[2,3-d][1,3]oxazine-2,4-dione;97484-73-6;1-benzyl-2H-pyrido[2,3-d][1,3]oxazine-2,4(1H)-dione;1-benzylpyrido[2,3-d][1,3]oxazine-2,4-dione;SCHEMBL1522698;DTXSID60540437;IOTFENHDTBFXDO-UHFFFAOYSA-N;AC9439;MFCD17011893;AKOS015839135;SY253988;CS-0098959;1-benzyl-1H,2H,4H-pyrido[2,3-d][1,3]oxazine-2,4-dione

Chemical Property of 1-Benzyl-1H-pyrido[2,3-d][1,3]oxazine-2,4-dione

Chemical Property:

• Vapor Pressure: 0mmHg at 25°C
• PSA: 65.10000
• LogP: 1.39800
• XLogP3: 2
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 2
• Exact Mass: 254.06914219
• Heavy Atom Count: 19
• Complexity: 366

Purity/Quality:

97% ^*data from raw suppliers

1-Benzyl-1H-pyrido[2,3-d][1,3]oxazine-2,4-dione 95% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C(C=C1)CN2C3=C(C=CC=N3)C(=O)OC2=O

Technology Process of 1-Benzyl-1H-pyrido[2,3-d][1,3]oxazine-2,4-dione

There total 6 articles about 1-Benzyl-1H-pyrido[2,3-d][1,3]oxazine-2,4-dione 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: 79.0%

benzyl chloride (100-44-7) + 3-azaisatoic anhydride (21038-63-1) → N-benzyl-2H-pyrido<2,3-d><1.3>oxazine-2,4 1H-dione (97484-73-6)

Guidance literature:

With sodium hydride; In N,N-dimethyl-formamide; for 3h; Ambient temperature;

DOI:10.1016/S0040-4020(01)90000-6

Reference yield: 68.0%

2-(benzylamino)nicotinic acid (33522-80-4) + trichloromethyl chloroformate (503-38-8) → N-benzyl-2H-pyrido<2,3-d><1.3>oxazine-2,4 1H-dione (97484-73-6)

Guidance literature:

In 1,4-dioxane; for 8h; Heating / reflux;

Reference yield: 51.0%

→ N-benzyl-2H-pyrido<2,3-d><1.3>oxazine-2,4 1H-dione (97484-73-6)

Guidance literature:

upstream raw materials:

benzyl chloride

3-azaisatoic anhydride

2-Aminocarbonylnicotinic acid

2-(benzylamino)nicotinic acid

Downstream raw materials:

2,3-dihydro-10-phenylmethylimidazo<1,2-a>pyrido<2,3-d>pyrimidin-5(10H)-one

1-(2'-benzylamino-3'-pyridinyl) cyclopentanol

1-(2'-benzylamino-3'-pyridinyl) cyclohexanol

1-benzyl-3-(1,1-dioxido-4H-1,2,4-benzothiadiazin-3-yl)-4-hydroxy-1,8-naphthyridin-2(1H)-one