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20348-21-4

20348-21-4 Structure

20348-21-4 Structure
IdentificationBack Directory
[Name]

2,2-dimethyl-2H-pyrido[3,2-b]-1,4-oxazin-3(4H)-one
[CAS]

20348-21-4
[Synonyms]

Einecs 243-753-2
2,2-dimethyl-4H-pyrido[3,2-b][1,4]oxazin-3-one
2,2-dimethyl-4H-pyrido[2,3-e][1,4]oxazin-3-one
2,2-Dimethyl-2H-pyrido[3,2-b][1,4]oxazin-3(4H)
2,2-dimethyl-2H-pyrido[3,2-b]-1,4-oxazin-3(4H)-one
2,2-DIMETHYL-2H-PYRIDO(3,2-B)(1,4)OXAZINE-3(4H)-ONE
2,2-diMethyl-2H,3H,4H-pyrido[3,2-b][1,4]oxazin-3-one
2H-Pyrido[3,2-b]-1,4-oxazin-3(4H)-one, 2,2-diMethyl-
[EINECS(EC#)]

243-753-2
[Molecular Formula]

C9H10N2O2
[MDL Number]

MFCD10000810
[MOL File]

20348-21-4.mol
[Molecular Weight]

178.188
Chemical PropertiesBack Directory
[Boiling point ]

352.5±37.0 °C(Predicted)
[density ]

1.176±0.06 g/cm3 (20 ºC 760 Torr)
[storage temp. ]

Store at room temperature
[form ]

solid
[pka]

11.13±0.40(Predicted)
[Appearance]

White to off-white Solid
[InChI]

InChI=1S/C9H10N2O2/c1-9(2)8(12)11-7-6(13-9)4-3-5-10-7/h3-5H,1-2H3,(H,10,11,12)
[InChIKey]

DMLNXUUGRSBBBR-UHFFFAOYSA-N
[SMILES]

O1C(C)(C)C(=O)NC2=NC=CC=C12
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302
[Precautionary statements ]

P301+P312+P330
[REACH Registrations]

Active
[HS Code ]

2934999090
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Acute Tox. 4 Oral
Spectrum DetailBack Directory
[Spectrum Detail]

2,2-dimethyl-2H-pyrido[3,2-b]-1,4-oxazin-3(4H)-one(20348-21-4)1HNMR
Hazard InformationBack Directory
[Synthesis]

2-Amino-3-hydroxypyridine

16867-03-1

Ethyl 2-bromoisobutyrate

600-00-0

2,2-dimethyl-2H-pyrido[3,2-b]-1,4-oxazin-3(4H)-one

20348-21-4

Step - (i): Synthesis of 2,2-dimethyl-2H-pyrido[3,2-B][1,4]oxazin-3(4H)-one (18.1) 2-Amino-3-hydroxypyridine (5 g, 45.45 mmol) was dissolved in acetone (50 mL) at 20-35 °C and stirred to form a solution. Subsequently K2CO3 (25.09g, 181.81mmol) was added followed by dropwise addition of ethyl 2-bromo-2-methylpropionate (13.29g, 68.18mmol). The reaction mixture was stirred at 70 °C for 16 hours. After completion of the reaction, the mixture was cooled to 20-35 °C and diluted with ice water. The resulting solid was collected by filtration and washed with water to afford the target compound as a white solid (5g, 97% yield). 1H NMR (400MHz, DMSO-d6): [specific NMR data should be added here].

[References]

[1] Patent: WO2015/71780, 2015, A1. Location in patent: Page/Page column 22
[2] Tetrahedron Letters, 2010, vol. 51, # 14, p. 1852 - 1855
[3] Acta Chemica Scandinavica (1947-1973), 1969, vol. 23, p. 2322 - 2324
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