Sodium Carbonate → HCID 53847360, compound
Reaction equation
[Cl:1][C:2]1[C:3]2[O:10][C:9]([C:11]([OH:13])=O)=[CH:8][C:4]=2[CH:5]=[N:6][CH:7]=1.S(Cl)([Cl:16])=O.C(=O)([O-])[O-].[Na+].[Na+]>ClCCl>[Cl:1][C:2]1[C:3]2[O:10][C:9]([C:11]([Cl:16])=[O:13])=[CH:8][C:4]=2[CH:5]=[N:6][CH:7]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
7-Chloro-furo[3,2-c]pyridine-2-carboxylic acid (prepared according to the method of Example 132, Step A, 8.94 g, 45.2 mmol) was combined with thionyl chloride (30 mL) and sodium carbonate (9.59 g, 90.5 mmol) and heated to reflux for 16 h under nitrogen atmosphere. The cooled mixture was diluted with dichloromethane and filtered. The filtrate was evaporated to give the title compound of Example 132, Step B as an orange oil, 9.19 g (94%). The acid chloride was used directly without further purification.
Workup
- temperatureheated
- temperatureto reflux for 16 h under nitrogen atmosphere
- filtrationfiltered
- customThe filtrate was evaporated
Sources & evidence
- ORD record
- ord-9f48f7d037664ff58f531488c74e6564
- Source dataset
- uspto-grants-2003_08
- Patent number
- US06602875B2
Reaction notes
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