Sodium Hydroxide → HCID 59403049, compound

HRID 415600Notes

Reaction equation

HRID 415600 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

6

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

  1. customto come to RT
  2. stirringstirred for 1 hr
  3. extractionextracted with dichloromethane (3×30 ml)
  4. customThe solvent was evaporated
  5. customto yield crude product, which
  6. 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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