Hydrochloric Acid → HCID 10293123, compound

HRID 1861017Notes

Reaction equation

HRID 1861017 reaction equation
[NH2:1][CH2:2][CH2:3][S:4]([C:6]1[CH:7]=[C:8]([C:20]2[NH:21][CH:22]=[CH:23][CH:24]=2)[C:9]2[C:10](=[O:19])[NH:11][C:12]3[C:17]=2[C:16]=1[C:15]([F:18])=[CH:14][CH:13]=3)=[O:5].[ClH:25]>CN(C=O)C.CO>[ClH:25].[NH2:1][CH2:2][CH2:3][S:4]([C:6]1[CH:7]=[C:8]([C:20]2[NH:21][CH:22]=[CH:23][CH:24]=2)[C:9]2[C:10](=[O:19])[NH:11][C:12]3[C:17]=2[C:16]=1[C:15]([F:18])=[CH:14][CH:13]=3)=[O:5]

Participants

5

Procedure

A solution of 5-(2-amino-ethanesulfinyl)-6-fluoro-3-(1H-pyrrol-2-yl)-1H-benzo[cd]indol-2-one (from Example 42 above) (20 mg, 0.06 mmol) in DMF (approximately 2.5 mL) was treated with aqueous HCl with vigorous stirring. The solution was lyophilized and the residue was dissolved in methanol, filtered and concentrated. The resulting material was further purified by precipitation out of MeOH/CH2Cl2 (3:1) with excess of pentane to give 5-(2-amino-ethanesulfinyl)-6-fluoro-3-(1H-pyrrol-2-yl)-1H-benzo[cd]indol-2-one hydrochloride salt as an orange solid. (Yield 19 mg, 77%).

Workup

  1. filtrationfiltered
  2. concentrationconcentrated
  3. customThe resulting material was further purified by precipitation out of MeOH/CH2Cl2 (3:1) with excess of pentane

Sources & evidence

ORD record
ord-cb747773113842f2b3ed8ae982748f79
Source dataset
uspto-grants-2003_03
Patent number
US06531598B1

Reaction notes

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