2-Propanone, 1-nitro- → HCID 15676508, compound

HRID 1589858Notes

Reaction equation

HRID 1589858 reaction equation
[C:1]1([C:7]2[S:8][C:9]3[C:15]([CH:16]=O)=[CH:14][CH:13]=[CH:12][C:10]=3[N:11]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[N+:18]([CH2:21][C:22](=O)[CH3:23])([O-:20])=[O:19].[NH2:25]/[C:26](/[CH3:32])=[CH:27]\[C:28]([O:30][CH3:31])=[O:29]>C(O)C>[CH3:23][C:22]1[NH:25][C:26]([CH3:32])=[C:27]([C:28]([O:30][CH3:31])=[O:29])[CH:16]([C:15]2[C:9]3[S:8][C:7]([C:1]4[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=4)=[N:11][C:10]=3[CH:12]=[CH:13][CH:14]=2)[C:21]=1[N+:18]([O-:20])=[O:19]

Participants

5

Procedure

10 mmol of 2-phenyl-benzothiazole-7-carboxaldehyde, 10 mmol of nitroacetone and 10 mmol of methyl 3-aminocrotonate are boiled in 20 ml of ethanol overnight, the mixture is concentrated and the residue is purified on a silica gel column (cyclohexane/ethyl acetate=6:4)

Workup

  1. concentrationthe mixture is concentrated
  2. customthe residue is purified on a silica gel column (cyclohexane/ethyl acetate=6:4)

Sources & evidence

ORD record
ord-f9c53ca12c5b4f2c82b9d705ecf672a3
Source dataset
uspto-grants-1993_04
Patent number
US05200420

Reaction notes

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