Sodium Carbonate → HCID 178430466, compound

HRID 1807621Notes

Reaction equation

HRID 1807621 reaction equation
[CH3:1][C:2]1[CH:9]=[N:8][CH:7]=[CH:6][C:3]=1[C:4]#[N:5].Cl.[NH2:11][OH:12].C([O-])([O-])=O.[Na+].[Na+]>CCO>[OH:12][NH:11][C:4](=[NH:5])[C:3]1[CH:6]=[CH:7][N:8]=[CH:9][C:2]=1[CH3:1]

Participants

5

Conditions

Temperature
85 °C

Procedure

Prepared using General Procedure 1. To 3-methylisonicotinonitrile (0.500 g, 4.2 mmol) in EtOH (7 mL) was added hydroxylamine hydrochloride (0.588 g, 8.5 mmol) and Na2CO3 (1.34 g, 12.7 mmol) and the reaction mixture was heated at 85° C. for 4 h. Once cooled to room temperature, the reaction mixture was filtered using EtOH to rinse the filter cake. The filtrate was concentrated under reduced pressure. The resulting pale yellow solid was triturated with ice water (50 mL), filtered, and the solid was washed with ice water (5 mL). The solid was dried under reduced pressure to yield 0.47 g (74%) of N-hydroxy-3-methylisonicotinimidamide INT-69 as a white powder. LCMS-ESI (m/z) calculated for C7H9N3O: 151.2; found 152.1 [M+H]+, tR=0.56 min. 1H NMR (400 MHz, CD3OD) δ 8.43-8.32 (m, 2H), 7.34 (d, J=5.0, 1H), 2.39 (s, 3H).

Workup

  1. customPrepared
  2. temperatureOnce cooled to room temperature
  3. filtrationthe reaction mixture was filtered
  4. washto rinse the filter cake
  5. concentrationThe filtrate was concentrated under reduced pressure
  6. customThe resulting pale yellow solid was triturated with ice water (50 mL)
  7. filtrationfiltered
  8. washthe solid was washed with ice water (5 mL)
  9. customThe solid was dried under reduced pressure

Sources & evidence

ORD record
ord-0b2713a95a5c4e30b8f3ee96d57ca3c0
Source dataset
uspto-grants-2013_01
Patent number
US08357706B2

Reaction notes

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