8H-Imidazo[2,1-c][1,4]oxazine-2-carboxaldehyde, 5,6-dihydro- (9CI)
- Product Name
- 8H-Imidazo[2,1-c][1,4]oxazine-2-carboxaldehyde, 5,6-dihydro- (9CI)
- CAS No.
- 623564-42-1
- Chemical Name
- 8H-Imidazo[2,1-c][1,4]oxazine-2-carboxaldehyde, 5,6-dihydro- (9CI)
- Synonyms
- 5,6-dihydro- (9CI);5H,6H,8H-imidazo[2,1-c][1,4]oxazine-2-carbaldehyde;5,6-Dihydro-8H-imidazo[2,1-c][1,4]oxazine-2-carbaldehyde;6,8-Dihydro-5H-imidazo[2,1-c]-[1,4]oxazine-2-carbaldehyde;5,6-Dihydro-8H-imidazo[2,1-c][1,4]oxazine-2-carboxaldehyde;8H-Imidazo[2,1-c][1,4]oxazine-2-carboxaldehyde, 5,6-dihydro-;8H-Imidazo[2,1-c][1,4]oxazine-2-carboxaldehyde, 5,6-dihydro- (9CI)
- CBNumber
- CB91090636
- Molecular Formula
- C7H8N2O2
- Formula Weight
- 152.15
- MOL File
- 623564-42-1.mol
8H-Imidazo[2,1-c][1,4]oxazine-2-carboxaldehyde, 5,6-dihydro- (9CI) Property
- Boiling point:
- 413.7±35.0 °C(Predicted)
- Density
- 1.41±0.1 g/cm3(Predicted)
- storage temp.
- under inert gas (nitrogen or Argon) at 2-8°C
- pka
- 2.72±0.20(Predicted)
- Appearance
- Light yellow to yellow Solid
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H317May cause an allergic skin reaction
H319Causes serious eye irritation
- Precautionary statements
-
P280Wear protective gloves/protective clothing/eye protection/face protection.
P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
N-Bromosuccinimide Price
- Product number
- D495820
- Product name
- 6,8-Dihydro-5H-imidazo[2,1-c][1,4]oxazine-2-carbaldehyde
- Packaging
- 50mg
- Price
- $130
- Updated
- 2021/12/16
- Product number
- FD148037
- Product name
- 5,6-Dihydro-8H-imidazo[2,1-c] [1,4]oxazine-2-carboxaldehyde
- Packaging
- 50mg
- Price
- $130
- Updated
- 2021/12/16
- Product number
- FD148037
- Product name
- 5,6-Dihydro-8H-imidazo[2,1-c] [1,4]oxazine-2-carboxaldehyde
- Packaging
- 100mg
- Price
- $200
- Updated
- 2021/12/16
- Product number
- FD148037
- Product name
- 5,6-Dihydro-8H-imidazo[2,1-c] [1,4]oxazine-2-carboxaldehyde
- Packaging
- 250mg
- Price
- $400
- Updated
- 2021/12/16
- Product number
- FD148037
- Product name
- 5,6-Dihydro-8H-imidazo[2,1-c] [1,4]oxazine-2-carboxaldehyde
- Packaging
- 500mg
- Price
- $600
- Updated
- 2021/12/16
8H-Imidazo[2,1-c][1,4]oxazine-2-carboxaldehyde, 5,6-dihydro- (9CI) Chemical Properties,Usage,Production
Synthesis
623564-41-0
623564-42-1
623564-43-2
Step 5: Synthesis of 5,6-dihydro-8H-imidazo[2,1-c][1,4]oxazine-2-carboxaldehyde (9) and 6,8-dihydro-5H-imidazo[2,1-c][1,4]oxazine-3-carboxaldehyde; a mixture of 2-bromo-3-hydroxyacrylaldehyde (4.1 g), p-toluenesulfonic acid monohydrate (52 mg) and 2-propanol (5.2 mL) in cyclohexane (42 mL ) in a mixture was subjected to azeotropic dehydration until the vapor temperature rose to 80 °C. The reaction mixture was concentrated under reduced pressure and the residue was dissolved in anhydrous ethanol (50 mL). To this solution was added a mixture of a solution of 3-iminomorpholine hydrochloride (3.4 g) in anhydrous ethanol (200 mL) and a methanol solution of 28% sodium methanol (4.8 g) at room temperature. The reaction mixture was stirred at room temperature for 2 hours before the solvent was removed under vacuum. The residue was dissolved in chloroform (125 mL), triethylamine (3.5 mL) was added and the reaction mixture was subsequently heated to reflux for 2 hours. After cooling to room temperature, the reaction mixture was concentrated under reduced pressure. The residue was dissolved in dichloromethane (300 mL) and washed with 50% aqueous K2CO3 (2 x 100 mL). The organic layer was dried over anhydrous magnesium sulfate and filtered, and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography using CHCl3-acetone (4:1) as eluent to afford the target product 5,6-dihydro-8H-imidazo[2,1-c][1,4]oxazine-2-carboxaldehyde (light orange solid, 1.4 g, 36.3% yield) and another regional isomer 6,8-dihydro-5H-imidazo[2,1-c][1,4]oxazine-3 -formaldehyde (light orange solid, 609 mg, 16.1% yield). 1H NMR (CDCl3) δ of the target product: 4.08-4.15 (m, 4H), 4.88 (s, 2H), 7.58 (s, 1H), 9.85 (s, 1H). 1H NMR (CDCl3) δ of the regional isomer: 4.06 (t, 2H, J=5.2Hz), 4.40 (t, 2H, J=5.2Hz), 4.90 (s, 2H), 7.75 (s, 1H), 9.72 (s, 1H).
References
[1] Patent: WO2003/93279, 2003, A1. Location in patent: Page/Page column 65-66
8H-Imidazo[2,1-c][1,4]oxazine-2-carboxaldehyde, 5,6-dihydro- (9CI) Preparation Products And Raw materials
Raw materials
Preparation Products
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