Hydrochloric Acid → HCID 15451836, compound
Reaction equation
[F:1][C:2]1([F:21])[O:6][C:5]2[CH:7]=[CH:8][C:9]([N:11]3[CH2:15][C:14](=[CH2:16])[S:13]/[C:12]/3=[N:17]\C(=O)C)=[CH:10][C:4]=2[O:3]1.Cl>C(O)C.O>[F:21][C:2]1([F:1])[O:6][C:5]2[CH:7]=[CH:8][C:9]([N:11]3[CH:15]=[C:14]([CH3:16])[S:13][C:12]3=[NH:17])=[CH:10][C:4]=2[O:3]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of Example 5 (1.8 g, 5.76 mmol) and hydrochloric acid (38%, 4.76 mL) in 40 mL of ethanol-water (1:1) was refluxed for 15 hours. Then the solvent was removed under reduced pressure, and the residue was carried on to the next step. 1H NMR (CD3OD) δ ppm 2.28 (3H), 7.15 (1H), 7.40-7.65 (3H); MS (ESI) 271 (M+H).
Workup
- customThen the solvent was removed under reduced pressure
Sources & evidence
- ORD record
- ord-4e3be9f012d44bb1b1cbc31ed41187b2
- Source dataset
- uspto-grants-2010_03
- Patent number
- US07683084B2
Reaction notes
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