3,4-Dihydro-2H-pyrido[3,2-b][1,4]oxazine-7-carbonitrile

Base Information

• Chemical Name: 3,4-Dihydro-2H-pyrido[3,2-b][1,4]oxazine-7-carbonitrile
• CAS No.: 34945-66-9
• Molecular Formula: C8H7N3O
• Molecular Weight: 161.16
• Hs Code.: 2934999090
• DSSTox Substance ID: DTXSID90587794
• Nikkaji Number: J3.049.869K
• Wikidata: Q82480292
• Mol file: 34945-66-9.mol

Synonyms:3,4-Dihydro-2H-pyrido[3,2-b][1,4]oxazine-7-carbonitrile;34945-66-9;SCHEMBL14376061;DTXSID90587794;2H-Pyrido[3,2-b]-1,4-oxazine-7-carbonitrile, 3,4-dihydro-;AKOS015995274;DB-069094;J-511181

Chemical Property of 3,4-Dihydro-2H-pyrido[3,2-b][1,4]oxazine-7-carbonitrile

Chemical Property:

• PSA: 57.94000
• LogP: 0.89558
• XLogP3: 0.6
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 0
• Exact Mass: 161.058911855
• Heavy Atom Count: 12
• Complexity: 210

Purity/Quality:

98% ^*data from raw suppliers

3,4-Dihydro-2H-pyrido[3,2-b][1,4]oxazine-7-carbonitrile 95+% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1COC2=C(N1)N=CC(=C2)C#N

Technology Process of 3,4-Dihydro-2H-pyrido[3,2-b][1,4]oxazine-7-carbonitrile

There total 7 articles about 3,4-Dihydro-2H-pyrido[3,2-b][1,4]oxazine-7-carbonitrile 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: 90.0%

potassiumhexacyanoferrate(II) trihydrate + 7-bromo-3,4-dihydro-2H-pyrido[3,2-β][1,4]oxazine (34950-82-8) → 3,4-dihydro-2H-pyrido-[3,2-b][1,4]oxazine-7-carbonitrile (34945-66-9)

Guidance literature:

With tetrakis(triphenylphosphine) palladium⁽⁰⁾; 1,8-diazabicyclo[5.4.0]undec-7-ene; In water; tert-butyl alcohol; at 85 ℃; for 4h; Inert atmosphere;

DOI:10.1039/c2cc17468e

Reference yield:

1-(7-bromo-2H-pyrido[3,2-b][1,4]oxazin-4 (3H)-yl)ethyl ketone (566158-30-3) + dicyanozinc (557-21-1) → 3,4-dihydro-2H-pyrido-[3,2-b][1,4]oxazine-7-carbonitrile (34945-66-9)

Guidance literature:

With zinc; 1,1'-bis-(diphenylphosphino)ferrocene; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; In N,N-dimethyl acetamide; at 150 ℃;

DOI:10.1021/jm070299x

Reference yield:

2-amino-3-hydroxypyridine (16867-03-1) → 3,4-dihydro-2H-pyrido-[3,2-b][1,4]oxazine-7-carbonitrile (34945-66-9)

Guidance literature:

Multi-step reaction with 4 steps

1: 89 percent / pyridine / 0.08 h / Heating

2: 99 percent / potassium carbonate / H₂O; acetone / Heating

3: N-bromosuccinimide / dimethylformamide / 1 h / 75 °C

4: 0.183 g / zinc / tris(dibenzylideneacetone)dipalladium⁽⁰⁾; 1,1'-bis(diphenylphosphino)ferrocene / N,N-dimethyl-acetamide / 150 °C

With pyridine; N-Bromosuccinimide; potassium carbonate; zinc; 1,1'-bis-(diphenylphosphino)ferrocene; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; In N,N-dimethyl acetamide; water; N,N-dimethyl-formamide; acetone;

DOI:10.1021/jm070299x

upstream raw materials:

copper(I) cyanide

7-bromo-3,4-dihydro-2H-pyrido[3,2-β][1,4]oxazine

1-(7-bromo-2H-pyrido[3,2-b][1,4]oxazin-4 (3H)-yl)ethyl ketone

dicyanozinc

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