Pyridine → HCID 86620600, compound
Reaction equation
C(Cl)(=O)C(Cl)=O.[C:7]([C:10]1[CH:40]=[CH:39][C:13]([O:14][CH2:15][C:16]2[CH:21]=[CH:20][C:19]([CH:22]([O:32][CH:33]3[CH2:38][CH2:37][CH2:36][CH2:35][O:34]3)[C:23]3[CH:24]=[C:25]([CH:29]=[CH:30][CH:31]=3)[C:26]([OH:28])=[O:27])=[CH:18][CH:17]=2)=[C:12]([CH3:41])[C:11]=1[OH:42])(=[O:9])[CH3:8].N1C=CC=CC=1.[NH2:49][NH:50][C:51]([NH2:53])=[S:52]>O1CCCC1.CN(C)C=O.CC(C)=O.O>[NH2:49][NH:50][C:51]([NH2:53])=[S:52].[C:7]([C:10]1[CH:40]=[CH:39][C:13]([O:14][CH2:15][C:16]2[CH:21]=[CH:20][C:19]([CH:22]([O:32][CH:33]3[CH2:38][CH2:37][CH2:36][CH2:35][O:34]3)[C:23]3[CH:24]=[C:25]([CH:29]=[CH:30][CH:31]=3)[C:26]([OH:28])=[O:27])=[CH:18][CH:17]=2)=[C:12]([CH3:41])[C:11]=1[OH:42])(=[O:9])[CH3:8]Participants
8
Reactant 4
Product 1
Reagents, catalysts & solvents 3
Procedure
Add oxalyl chloride (0.660 mg, 5.20 mmol) to a solution of 3-[[4-(4-acetyl-3-hydroxy-2-methyl-phenoxymethyl)-phenyl]-(tetrahydro-pyran-2-yloxy)-methyl]-benzoic acid, 1.00 g, 2.04 mmol) in tetrahydrofuran (0.20M). Add dimethylformamide (5 drops). Add pyridine (0.322 g, 4.08 mmol) and thiosemicarbazide (0.223 g, 2.45 mmol). Stir the reaction overnight. Evaporate solvents. Dissolve brown tar in acetone/water. Extract with CH2Cl2 (3×) and ethyl acetate (3×). Combine organic extracts, dry and concentrate to afford the title compound, which was used without further purification (1.20 g, 2.04 mmol, 99%): MS (m/z): 563 (M−H).
Workup
- customthe reaction overnight
- extractionExtract with CH2Cl2 (3×) and ethyl acetate (3×)
- customCombine organic extracts, dry
- concentrationconcentrate
Sources & evidence
- ORD record
- ord-20f489b857f1425c9f446c64abc8d677
- Source dataset
- uspto-grants-2009_10
- Patent number
- US07598423B2
Reaction notes
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