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20348-23-6

20348-23-6 Structure

20348-23-6 Structure
IdentificationBack Directory
[Name]

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

20348-23-6
[Synonyms]

2H,3H,4H-pyrido[3,2-b][1,4]oxazine
3,4-Dihydro-2H-pyrido[3,2-b]oxazine
2,3-dihydropyrido[3,2-b][1,4]oxazine
3,4-DIHYDRO-2H-PYRIDO[3,2-B][1,4]OXAZINE
2H-Pyrido[3,2-b]-1,4-oxazine, 3,4-dihydro-
3,4-Dihydro-2H-pyrido[3,2-b][1,4]oxazine ISO 9001:2015 REACH
[Molecular Formula]

C7H8N2O
[MDL Number]

MFCD09025907
[MOL File]

20348-23-6.mol
[Molecular Weight]

136.151
Chemical PropertiesBack Directory
[Melting point ]

85 °C
[Boiling point ]

285.7±29.0 °C(Predicted)
[density ]

1.168
[storage temp. ]

2-8°C(protect from light)
[pka]

9.82±0.20(Predicted)
[Appearance]

White to off-white Solid
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302+H312+H332-H315-H319-H335
[Precautionary statements ]

P261-P280-P305+P351+P338
[HazardClass ]

IRRITANT
[HS Code ]

2933399990
Hazard InformationBack Directory
[Definition]

ChEBI: 3,4-Dihydro-2H-pyrido[3,2-b][1,4]oxazine is a secondary amine.
[Synthesis]

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

20348-09-8

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

20348-23-6

(a) Synthesis of 3,4-dihydro-2H-pyrido[3,2-b][1,4]oxazine: To a solution of 2H-pyrido[3,2-b][1,4]oxazin-3(4H)-one (5.00 g, 33.3 mmol) in tetrahydrofuran (THF, 40 mL) was slowly added lithium aluminium hydroxide (66.6 mL, 1.0 M THF solution. 66.6 mmol). After addition, the reaction mixture was heated to reflux. After 18 hours of reaction, the reaction was cooled to 0 °C and water (4 mL), sodium hydroxide solution (4 mL, 15%) and water (10 mL) were added sequentially to quench the reaction. Subsequently, the reaction mixture was filtered through diatomaceous earth and the filtrate was concentrated to afford the target product 3,4-dihydro-2H-pyrido[3,2-b][1,4]oxazine (3.87 g, 85% yield) as a blue-gray powder. The product was characterized by 1H NMR (500 MHz, DMSO-d6): δ 7.53 (dd, J=4.5,1.0 Hz, 1H), 6.90-6.89 (m, 1H), 6.61 (br s, 1H), 6.44 (dd, J=8.0,3.0 Hz, 1H), 4.08 (t, J=4.5 Hz, 2H), 3.39- 3.36 (m, 2H); mass spectrum (ESI) m/e 131 (M+H)+.

[References]

[1] Patent: WO2007/53131, 2007, A2. Location in patent: Page/Page column 133
[2] Patent: EP1226138, 2004, B1
[3] Acta Chemica Scandinavica (1947-1973), 1969, vol. 23, p. 2322 - 2324
[4] Patent: US2008/305169, 2008, A1
[5] Patent: US2007/10670, 2007, A1. Location in patent: Page/Page column 92
Spectrum DetailBack Directory
[Spectrum Detail]

3,4-Dihydro-2H-pyrido[3,2-b][1,4]oxazine(20348-23-6)1HNMR
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