Chloroform → HCID 70155363, compound

HRID 1683482Notes

Reaction equation

HRID 1683482 reaction equation
[CH2:1]([C@:3]1([OH:41])[C:38]2[CH:37]=[C:36]3[N:9]([CH2:10][C:11]4[C:12]3=[N:13][C:14]3[CH:15]=[CH:16][C:17]([F:35])=[C:18]5[CH:23]([N:24]6C(=O)C7C(=CC=CC=7)C6=O)[CH2:22][CH2:21][C:20]=4[C:19]=35)[C:8](=[O:39])[C:7]=2[CH2:6][O:5][C:4]1=[O:40])[CH3:2].O.NN.C(Cl)(Cl)[Cl:46]>CO>[ClH:46].[NH2:24][CH:23]1[C:18]2[C:19]3[C:20](=[C:11]4[CH2:10][N:9]5[C:36](=[CH:37][C:38]6[C@:3]([CH2:1][CH3:2])([OH:41])[C:4](=[O:40])[O:5][CH2:6][C:7]=6[C:8]5=[O:39])[C:12]4=[N:13][C:14]=3[CH:15]=[CH:16][C:17]=2[F:35])[CH2:21][CH2:22]1

Participants

5

Procedure

120 mg of the compound prepared in (11) above was dissolved in a mixed solvent of 7 ml of chloroform and 5 ml of methanol. After the addition of 0.7 ml of hydrazine monohydrate, the mixture was heated under reflux for 1 hour. The reaction mixture was concentrated to dryness and to the residue was added 7 ml of 4N hydrochloric acid, and the mixture was heated under reflux for 1 hour. After concentration to dryness, 10 ml of water to the residue to remove the insoluble substances by filtration. The filtrate was purified in the same manner as in Example 7 to obtain 32 mg of Isomer A and 20 mg of Isomer B of the title compound.

Workup

  1. temperaturethe mixture was heated
  2. temperatureunder reflux for 1 hour
  3. concentrationThe reaction mixture was concentrated to dryness and to the residue
  4. additionwas added 7 ml of 4N hydrochloric acid
  5. temperaturethe mixture was heated
  6. temperatureunder reflux for 1 hour
  7. concentrationAfter concentration to dryness, 10 ml of water to the residue
  8. customto remove the insoluble substances
  9. filtrationby filtration
  10. customThe filtrate was purified in the same manner as in Example 7

Sources & evidence

ORD record
ord-96bf3d031ec5478dae2fca6efaa9d241
Source dataset
uspto-grants-1997_06
Patent number
US05637770

Reaction notes

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