Methanol → HCID 67432359, compound

HRID 578046Notes

Reaction equation

HRID 578046 reaction equation
[BH4-].[Li+].CO.[F:5][C:6]1[C:7]2[O:32][N:31]=[C:30]([N:33]3[CH:37]=[C:36]([C:38](OCC)=[O:39])[CH:35]=[N:34]3)[C:8]=2[CH:9]=[C:10]2[C:23]=1[N:22]1[CH2:24][C@@H:25]([CH3:29])[O:26][C@@H:27]([CH3:28])[C@@H:21]1[C:12]1([C:17](=[O:18])[NH:16][C:15](=[O:19])[NH:14][C:13]1=[O:20])[CH2:11]2>O1CCCC1.O>[F:5][C:6]1[C:7]2[O:32][N:31]=[C:30]([N:33]3[CH:37]=[C:36]([CH2:38][OH:39])[CH:35]=[N:34]3)[C:8]=2[CH:9]=[C:10]2[C:23]=1[N:22]1[CH2:24][C@@H:25]([CH3:29])[O:26][C@@H:27]([CH3:28])[C@@H:21]1[C:12]1([C:17](=[O:18])[NH:16][C:15](=[O:19])[NH:14][C:13]1=[O:20])[CH2:11]2

Participants

6

Procedure

Lithium borohydride (0.434 mL, 0.87 mmol) was added to an ice cooled solution of methanol (0.035 mL, 0.87 mmol) in tetrahydrofuran (10 mL). The solution was warmed to room temp and stirred for 1 hour. 1.5 ml of this solution was added to a solution of ethyl 1-[(2R,4S,4aS)-11-fluoro-2,4-dimethyl-2′,4′,6′-trioxo-1,1′,2,3′,4,4′,4a,6′-octahydro-2′H,6H-spiro[1,4-oxazino[4,3-a][1,2]oxazolo[4,5-g]quinoline-5,5′-pyrimidin]-8-yl]-1H-pyrazole-4-carboxylate (Example 37, 60 mg, 0.11 mmol). The reaction was stirred at room temp for 12 hours. The reaction mixture was diluted with water and extracted twice with ethyl acetate. The organic layers were washed twice with brine, dried over MgSO4 and concentrated. The residue was purified by reverse phase HPLC to give product as a solid. Yield: 20 mg.

Workup

  1. stirringThe reaction was stirred at room temp for 12 hours
  2. extractionextracted twice with ethyl acetate
  3. washThe organic layers were washed twice with brine
  4. dry with materialdried over MgSO4
  5. concentrationconcentrated
  6. customThe residue was purified by reverse phase HPLC
  7. customto give product as a solid

Sources & evidence

ORD record
ord-ff5d3ddb11a34a688914a4c1465f1f7c
Source dataset
uspto-grants-2015_05
Patent number
US09040528B2

Reaction notes

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