Hydrochloric Acid → HCID 70212384, compound

HRID 619465Notes

Reaction equation

HRID 619465 reaction equation
[F:1][C:2]([F:29])([F:28])[S:3]([NH:6][C:7]1[CH:12]=[CH:11][C:10]([CH2:13][N:14]2[C:24](=[O:25])[C:23]3[N:26]4[C:16](=[CH:17][N:18]=[C:19]4[CH:20]=[CH:21][CH:22]=3)[C:15]2=[O:27])=[CH:9][CH:8]=1)(=[O:5])=[O:4].[ClH:30]>CO>[ClH:30].[F:28][C:2]([F:1])([F:29])[S:3]([NH:6][C:7]1[CH:12]=[CH:11][C:10]([CH2:13][N:14]2[C:24](=[O:25])[C:23]3[N:26]4[C:16](=[CH:17][N:18]=[C:19]4[CH:20]=[CH:21][CH:22]=3)[C:15]2=[O:27])=[CH:9][CH:8]=1)(=[O:4])=[O:5]

Participants

4

Procedure

To a suspension of 129 mg (0.30 mmol) of 4,5-dihydro-4-[4-(trifluoromethanesulfonamido) phenylmethyl]-3H-1,4,8b-triazaacenaphthylene-3,5-dione in 10 ml of methanol was added 0.04 ml of conc. HCl. The solvent was distilled off. To the residue was added acetone. The resulting solid was washed with acetone and dried to afford 141 mg of the desired compound (100%, a pale brown solid).

Workup

  1. distillationThe solvent was distilled off
  2. additionTo the residue was added acetone
  3. washThe resulting solid was washed with acetone
  4. customdried

Sources & evidence

ORD record
ord-b81648bd629c4aafb51598831b6ce47b
Source dataset
uspto-grants-1999_09
Patent number
US05958942

Reaction notes

Loading…