Potassium Hydroxide → HCID 178515829, compound
Reaction equation
F[C:2]1[CH:7]=[CH:6][C:5]([CH:8]2[CH2:13][CH:12]3[NH:14][CH:9]2[CH2:10][CH2:11]3)=[CH:4][N:3]=1.[OH-:15].[K+]>C(O)(C)(C)C>[OH:15][C:2]1[CH:7]=[CH:6][C:5]([CH:8]2[CH2:13][CH:12]3[NH:14][CH:9]2[CH2:10][CH2:11]3)=[CH:4][N:3]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Compound 53 (8.5 mg, 0.044 mmol) was dissolved in 1 ml tert-butanol. To this solution was added 1 ml 2M potassium hydroxide. After reflux for 20 hours and evaporation of butanol, the mixture was adjusted with 1M hydrochloric acid to pH 6-7. Evaporation of solvent in vacuo and purification of product with silica gel preparative thin layer chromatography developing with 20% 7N ammonia methanol in chloroform gave 4.2 mg compound 77 as an oil. Yield 50%. MS(CI) 191(M+1). 1H-NMR (CDCl3) δ2.554 (br.s., 1H, H2), 3.503; 3.743 (2br.s., 2H, H1,4).
Workup
- temperatureAfter reflux for 20 hours
- customevaporation of butanol
- customEvaporation of solvent
- customin vacuo and purification of product with silica gel preparative thin layer chromatography
Sources & evidence
- ORD record
- ord-dc8d31b9c34f4179a7e77f9e0adf4772
- Source dataset
- uspto-grants-2001_07
- Patent number
- US06255490B1
Reaction notes
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