Hydroxyamine hydrochloride → HCID 49823922, compound

HRID 1418504Notes

Reaction equation

HRID 1418504 reaction equation
[CH3:1][C:2]1[N:3]([C:7]2[CH:12]=[CH:11][C:10]([S:13][C:14]3[CH:15]=[C:16]([C:20]4([CH:26]=O)[CH2:25][CH2:24][O:23][CH2:22][CH2:21]4)[CH:17]=[CH:18][CH:19]=3)=[CH:9][CH:8]=2)[CH:4]=[CH:5][N:6]=1.Cl.[NH2:29][OH:30]>CO.N1C=CC=CC=1>[OH:30][N:29]=[CH:26][C:20]1([C:16]2[CH:17]=[CH:18][CH:19]=[C:14]([S:13][C:10]3[CH:11]=[CH:12][C:7]([N:3]4[CH:4]=[CH:5][N:6]=[C:2]4[CH3:1])=[CH:8][CH:9]=3)[CH:15]=2)[CH2:21][CH2:22][O:23][CH2:24][CH2:25]1

Participants

5

Procedure

4-[3-[4-(2-Methylimidazol-1-yl)phenylthio]phenyl]-3,4,5,6-tetrahydro-2H-pyran-4-carbaldehyde (178 mg, 0.47 mmol) and hydroxylamine hydrochloride (210 mg, 3 mmol) were dissolved in a mixture of methanol (4 ml) and pyridine (1 ml) and the reaction mixture was stirred for 5 h at ambient temperature. Volatiles were removed in vacuo and the resultant residue was diluted with 0.1N aqueous NaOH (20 ml) and extracted with ethyl acetate (30 ml×3). The combined organic layers were washed with water (50 ml) and brine (50 ml), dried (MgSO4) and concentrated in vacuo. The residual solids were recrystallized from ethyl acetate to afford 130 mg (70%) of the titled compound as white solids.

Workup

  1. customVolatiles were removed in vacuo
  2. additionthe resultant residue was diluted with 0.1N aqueous NaOH (20 ml)
  3. extractionextracted with ethyl acetate (30 ml×3)
  4. washThe combined organic layers were washed with water (50 ml) and brine (50 ml)
  5. dry with materialdried (MgSO4)
  6. concentrationconcentrated in vacuo
  7. customThe residual solids were recrystallized from ethyl acetate

Sources & evidence

ORD record
ord-d7205d3bcfc1440e92526b0248d576a9
Source dataset
uspto-grants-1999_03
Patent number
US05883106

Reaction notes

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