Hydrochloric Acid → HCID 46206436, compound
Reaction equation
[F:1][C:2]1[CH:7]=[C:6]([S:8][C:9]2[CH:14]=[CH:13][C:12]([CH:15]([CH3:17])[CH3:16])=[CH:11][CH:10]=2)[CH:5]=[CH:4][C:3]=1[C:18]1[CH:23]=[CH:22][C:21]([CH2:24][CH2:25][C:26]2([NH:34]C(=O)C)[CH2:31][O:30]C(C)(C)[O:28][CH2:27]2)=[CH:20][CH:19]=1.[ClH:38]>C(O)C>[ClH:38].[NH2:34][C:26]([CH2:25][CH2:24][C:21]1[CH:20]=[CH:19][C:18]([C:3]2[CH:4]=[CH:5][C:6]([S:8][C:9]3[CH:10]=[CH:11][C:12]([CH:15]([CH3:16])[CH3:17])=[CH:13][CH:14]=3)=[CH:7][C:2]=2[F:1])=[CH:23][CH:22]=1)([CH2:31][OH:30])[CH2:27][OH:28]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 75 °C
Procedure
N-(5-{2-[2′-Fluoro-4′-(4-isopropylphenylthio)biphenyl-4-yl]ethyl}-2,2-dimethyl-1,3-dioxan-5-yl)acetamide (0.24 g) was dissolved in ethanol (4 mL), concentrated hydrochloric acid (2 mL) was added, and the mixture was stirred at 75° C. for 4 hr. The reaction mixture was concentrated to dryness, and the residual solid was suspended in ethyl acetate and collected by filtration to give the title compound (141 mg) as white crystals.
Workup
- concentrationThe reaction mixture was concentrated to dryness
- filtrationcollected by filtration
Sources & evidence
- ORD record
- ord-b6175d396b694238a4142e78e468df3d
- Source dataset
- uspto-grants-2012_02
- Patent number
- US08114902B2
Reaction notes
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