Acetic Acid → 2-(1-neopentyl-2-oxo-2,3,4,7-tetrahydro-1H-pyrazolo[3,4-h]quinolin-3-yl)acetic acid

HRID 132173

Reaction equation

HRID 132173 reaction equation
[NH2:1][C:2]1[C:11]([CH3:12])=[C:10]2[C:5]([CH2:6][CH:7]([CH2:19][C:20]([O:22]CC)=[O:21])[C:8](=[O:18])[N:9]2[CH2:13][C:14]([CH3:17])([CH3:16])[CH3:15])=[CH:4][CH:3]=1.C(O)(=O)C.C(O[N:35]=O)CC(C)C.[OH-].[Li+]>C(Cl)(Cl)(Cl)Cl.ClCCl.O>[CH2:13]([N:9]1[C:10]2[C:5](=[CH:4][CH:3]=[C:2]3[NH:1][N:35]=[CH:12][C:11]3=2)[CH2:6][CH:7]([CH2:19][C:20]([OH:22])=[O:21])[C:8]1=[O:18])[C:14]([CH3:15])([CH3:17])[CH3:16]

Participants

8

Procedure

To a solution of ethyl 2-(7-amino-8-methyl-1-neopentyl-2-oxo-1,2,3,4-tetrahydroquinolin-3-yl)acetate (170 mg, 0.51 mmol) in carbon tetrachloride (4.5 mL) was added acetic acid (0.5 mL) followed by isoamylnitrite (0.04 mL) and the reaction mixture was stirred for 2 h at room temperature. The reaction mixture was diluted with dichloromethane (40 mL), washed with aqueous NaHCO3 and dried. The solvent was removed and the crude product was dissolved in THF (15 mL) followed by addition of lithium hydroxide (43 mg, 1 mmol) and water (5 mL). After stirring for 12 h, the solvent was removed, acidified with 6 M HCl and extracted with ethyl acetate to give 2-(1-neopentyl-2-oxo-2,3,4,7-tetrahydro-1H-pyrazolo[3,4-h]quinolin-3-yl)acetic acid.

Workup

  1. washwashed with aqueous NaHCO3
  2. customdried
  3. customThe solvent was removed
  4. dissolutionthe crude product was dissolved in THF (15 mL)
  5. stirringAfter stirring for 12 h
  6. customthe solvent was removed
  7. extractionextracted with ethyl acetate

Sources & evidence

ORD record
ord-34da6b580271408994b3aeb4f2a4f511
Source dataset
uspto-grants-2008_06
Patent number
US07384930B2

Linked notes

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