Sodium Hydroxide → 3,4-Dihydro-2H-pyrido[3,2-b]-1,4-oxazin-2-ylmethanol

HRID 1789728Notes

Reaction equation

C([O:3][C:4]([CH:6]1[O:11][C:10]2[CH:12]=[CH:13][CH:14]=[N:15][C:9]=2[NH:8][C:7]1=O)=O)C.[H-].[H-].[H-].[H-].[Li+].[Al+3].[OH-].[Na+]>C1COCC1>[O:11]1[CH:6]([CH2:4][OH:3])[CH2:7][NH:8][C:9]2[N:15]=[CH:14][CH:13]=[CH:12][C:10]1=2

Participants

Conditions

Temperature: 45 °C

Procedure

A solution of 3,4-dihydro-3-oxo-2H-pyrido[3,2-b]-1,4-oxazin-2-carboxylic acid ethyl ester (1.10 g, 5.0 mmol) in THF (50 mL) was added over 5 min to a stirred mixture of LiAlH4 (0.38 g, 10 mmol) and THF (20 mL) at 40° C. The mixture was stirred at 45° C. for 30 min and at reflux for 4 h. The mixture was allowed to attain room temperature and excess LiAlH4 decomposed with 50% aqueous NaOH. The mixture was filtered through Celite, and the filtrate was concentrated. The residue (0.42 g) was extracted with CH2Cl2 and the extract was concentrated and purified by chromatography on silica gel (gradient: PhMe to PhMe/MeOH/Et3N, 8:1:1) to give the product as a white solid: yield 0.11 g (13%); mp 123-124° C. Anal. (C8H10N2O2) C, H, N.

Workup

temperatureat reflux for 4 h
customto attain room temperature
filtrationThe mixture was filtered through Celite
concentrationthe filtrate was concentrated
extractionThe residue (0.42 g) was extracted with CH2Cl2
concentrationthe extract was concentrated
custompurified by chromatography on silica gel (gradient: PhMe to PhMe/MeOH/Et3N, 8:1:1)

Sources & evidence

ORD record: ord-505c56af85be4a3496e51b1ff750ab27
Source dataset: uspto-grants-2006_07
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US07071180B2

Reaction notes

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