Pyridine → HCID 86620600, compound

HRID 1818543Notes

Reaction equation

HRID 1818543 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

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

  1. customthe reaction overnight
  2. extractionExtract with CH2Cl2 (3×) and ethyl acetate (3×)
  3. customCombine organic extracts, dry
  4. concentrationconcentrate

Sources & evidence

ORD record
ord-20f489b857f1425c9f446c64abc8d677
Source dataset
uspto-grants-2009_10
Patent number
US07598423B2

Reaction notes

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