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60832-72-6

60832-72-6 Structure

60832-72-6 Structure
IdentificationMore
[Name]

2,3-Dihydropyrido[2,3-d][1,3]oxazol-2-one
[CAS]

60832-72-6
[Synonyms]

[1,3]Oxazolo[4,5-b]pyridin-2-ol
2,3-DIHYDROPYRIDO[2,3-D][1,3]OXAZOL-2-ONE
3H-OXAZOLO[4,5-B]PYRIDIN-2-ONE
oxazolo[4,5-6]pyridine-2(3h)-one
Oxazolo[4,5-b]pyridine-2(3H)one
oxazolo[4,5-b]pyridin-2(3H)-one
[Molecular Formula]

C6H4N2O2
[MDL Number]

MFCD00204215
[Molecular Weight]

136.11
[MOL File]

60832-72-6.mol
Chemical PropertiesBack Directory
[Melting point ]

214 °C
[Boiling point ]

253.8±23.0 °C(Predicted)
[density ]

1.59±0.1 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[solubility ]

DMSO, Methanol
[form ]

Solid
[pka]

2.76±0.20(Predicted)
[color ]

Tan
[InChI]

InChI=1S/C6H4N2O2/c9-6-8-5-4(10-6)2-1-3-7-5/h1-3H,(H,7,8,9)
[InChIKey]

OVLXOTUWFLHWQT-UHFFFAOYSA-N
[SMILES]

C12NC(=O)OC1=CC=CN=2
[CAS DataBase Reference]

60832-72-6(CAS DataBase Reference)
Safety DataBack Directory
[Hazard Codes ]

Xn
[Risk Statements ]

R20/21/22:Harmful by inhalation, in contact with skin and if swallowed .
R36/37/38:Irritating to eyes, respiratory system and skin .
[Safety Statements ]

S22:Do not breathe dust .
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection .
[Hazard Note ]

Harmful
[REACH Registrations]

Active
[HS Code ]

2934999090
Hazard InformationBack Directory
[Chemical Properties]

Tan Solid
[Uses]

2,3-Dihydropyrido[2,3-d][1,3]oxazol-2-one is a benzoxazolone analogue that may be used to inhibit the nitric oxide synthases (NOS).
[Definition]

ChEBI:Oxazolo[4,5-b]pyridin-2(3H)-one is a lactone. It derives from a hydride of an oxazolo[4,5-b]pyridine.
[Synthesis]

2-Amino-3-hydroxypyridine

16867-03-1

1,1'-Carbonyldiimidazole

530-62-1

2,3-Dihydropyrido[2,3-d][1,3]oxazol-2-one

60832-72-6

N,N'-Carbonyldiimidazole (57.4 g, 354.2 mmol) was slowly added to a tetrahydrofuran (THF) solution (400 mL) of 2-amino-3-hydroxypyridine (26.0 g, 236.1 mmol, purchased from Aldrich) as described in Step 4-i of Scheme 4. The resulting reaction mixture was stirred at 70 °C for 14 hours. Upon completion of the reaction, the mixture was cooled to room temperature and concentrated under reduced pressure. The concentrated residue was dissolved in dichloromethane (DCM) (500 mL) and subsequently washed with 2N sodium hydroxide (NaOH) solution (3 x 100 mL). The aqueous phases were combined, cooled to 0 °C, and the pH was adjusted to 6 with 6 N hydrochloric acid (HCl).At this point, the product precipitated as a precipitate, which was collected through a sintered funnel and washed with cold water (100 mL). Finally, the product was dried under vacuum to afford 2,3-dihydropyrido[2,3-d][1,3]oxazol-2-one (compound 1011, 26.0 g, 81% yield). The product was characterized by the following data: electrospray mass spectrometry (ESMS) (M + H) + m/z 137; 1H NMR (DMSO-d6) δ 12.4 (br, 1H), 8.0 (d, 1H), 7.6 (d, 1H), 7.1 (dd, 1H).

[References]

[1] Patent: WO2007/67416, 2007, A2. Location in patent: Page/Page column 56; 91
[2] Patent: WO2010/96389, 2010, A1. Location in patent: Page/Page column 42; 44
[3] Patent: WO2010/135014, 2010, A1. Location in patent: Page/Page column 50-51
[4] Journal of Medicinal Chemistry, 2015, vol. 58, # 20, p. 8066 - 8096
[5] Patent: WO2009/23844, 2009, A2. Location in patent: Page/Page column 120
Spectrum DetailBack Directory
[Spectrum Detail]

2,3-Dihydropyrido[2,3-d][1,3]oxazol-2-one(60832-72-6)1HNMR
Well-known Reagent Company Product InformationBack Directory
[Acros Organics]

[1,3]oxazolo[4,5-b]pyridin-2-ol(60832-72-6)
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