Hydroxyamine hydrochloride → HCID 178513307, compound

HRID 1840539Notes

Reaction equation

HRID 1840539 reaction equation
Cl[C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[CH:8]=[C:7]([S:12]([N:15]1[CH2:20][CH2:19][N:18]([CH2:21][C:22]3[CH:27]=[CH:26][C:25]([C:28]#[N:29])=[CH:24][CH:23]=3)[C:17](=[O:30])[CH2:16]1)(=[O:14])=[O:13])[CH:6]=[CH:5]2.[ClH:31].[NH2:32][OH:33].C(=O)([O-])O.[Na+]>C(O)C>[Cl:31][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[CH:8]=[C:7]([S:12]([N:15]1[CH2:20][CH2:19][N:18]([CH2:21][C:22]3[CH:23]=[CH:24][C:25]([C:28](=[NH:29])[NH:32][OH:33])=[CH:26][CH:27]=3)[C:17](=[O:30])[CH2:16]1)(=[O:14])=[O:13])[CH:6]=[CH:5]2

Participants

5

Procedure

A mixture of 4-(6-chloronaphthalene-2-sulfonyl)-1-(4-cyanobenzyl)-2-piperazinone (440 mg), hydroxylamine hydrochloride (347 mg), sodium hydrogen carbonate (420 mg) and 80% ethanol (30 ml) was refluxed for 2 hours, and ethanol was evaporated. Precipitated crystals were washed with water, ethanol and ethyl acetate, and dried to give colorless crystals of the title compound (353 mg).

Workup

  1. temperaturewas refluxed for 2 hours
  2. customethanol was evaporated
  3. customPrecipitated crystals
  4. washwere washed with water, ethanol and ethyl acetate
  5. customdried

Sources & evidence

ORD record
ord-b085c715a88c4080a9737bfc84e6ca56
Source dataset
uspto-grants-2004_01
Patent number
US06680312B2

Reaction notes

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