Hydrochloric Acid → HCID 90416278, compound
Reaction equation
[F:1][C:2]1[CH:35]=[C:34]([F:36])[CH:33]=[CH:32][C:3]=1[O:4][C:5]1[CH:10]=[CH:9][C:8]([NH:11][S:12]([CH2:15][CH3:16])(=[O:14])=[O:13])=[CH:7][C:6]=1[C:17]1[C:25]2[C:20](=[C:21]([O:29]C)[N:22]=[C:23]([C:26]([OH:28])=[O:27])[CH:24]=2)[N:19]([CH3:31])[CH:18]=1.Cl>O1CCOCC1>[F:1][C:2]1[CH:35]=[C:34]([F:36])[CH:33]=[CH:32][C:3]=1[O:4][C:5]1[CH:10]=[CH:9][C:8]([NH:11][S:12]([CH2:15][CH3:16])(=[O:14])=[O:13])=[CH:7][C:6]=1[C:17]1[C:25]2[CH:24]=[C:23]([C:26]([OH:28])=[O:27])[NH:22][C:21](=[O:29])[C:20]=2[N:19]([CH3:31])[CH:18]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of Example 187E (335 mg, 0.647 mmol), 4M hydrogen chloride in dioxane (2.0 mL, 8.00 mmol) and dioxane (10 mL) was stirred at 75° C. for 4 hours. The reaction mixture was cooled to ambient temperature and was concentrated to dryness. The residue was dried (in-vacuo) to provide 315 mg (97%) of the title compound.
Workup
- concentrationwas concentrated to dryness
- customThe residue was dried (in-vacuo)
Sources & evidence
- ORD record
- ord-83cf4607875d4f82bf55ca86a8b4deea
- Source dataset
- uspto-grants-2016_04
- Patent number
- US09321764B2
Reaction notes
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