Sodium Hydroxide → HCID 59403049, compound
Reaction equation
N[C:2]1[CH:3]=[C:4]([CH:8]=[C:9]([O:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH3:17])[CH:10]=1)[C:5]([NH2:7])=[O:6].N([O-])=O.[Na+].[OH-].[Na+].[F:24][B-](F)(F)F.[H+]>O>[F:24][C:2]1[CH:3]=[C:4]([CH:8]=[C:9]([O:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH3:17])[CH:10]=1)[C:5]([NH2:7])=[O:6]Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 60 °C
Procedure
To a solution of 3-amino-5-hexyloxy benzamide (0.9 g, 3.8 mmol) in tetrafluoroboric acid (20 ml), a solution of sodium nitrite (0.315 mg, 4.6 mmol) in water (5 ml) was added at 0° C. and stirred for 1 hr. Later it was allowed to come to RT and stirred for 1 hr followed by heating at 60° C. for 2 hrs. It was then basify to pH=14 using saturated NaOH solution and extracted with dichloromethane (3×30 ml). The solvent was evaporated to yield crude product, which was purified by column chromatography using silica gel (230-400 mesh) and dichloromethane as an eluent (100 mg, 11%). 1H NMR (DMSO-d6, 400 MHz with D2O): δ 0.88 (t, J=7.2 Hz, 3H), 1.32 (m, 2H), 1.41 (m, 4H), 1.72 (m, 2H), 4.0 (t, J=7.2 Hz, 2H), 6.97 (m, 1H), 7.22 (m, 1H), 7.28 (m, 1H), 7.52 (br s, 1H), 8.03 (br s, 1H). MS ES+ (238.0, 239.0), HPLC (method 7) Rt=11.34 min.
Workup
- customto come to RT
- stirringstirred for 1 hr
- extractionextracted with dichloromethane (3×30 ml)
- customThe solvent was evaporated
- customto yield crude product, which
- customwas purified by column chromatography
Sources & evidence
- ORD record
- ord-3cf7d53c03e5433481003389f20d965b
- Source dataset
- uspto-grants-2012_01
- Patent number
- US08088791B2
Reaction notes
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