Water → HCID 14390458, compound
Reaction equation
C([O:3][C:4](=[O:22])[CH2:5][NH:6][C:7]1[C:12]([NH:13][C:14]([C:16]2[O:17][C:18]([Br:21])=[CH:19][CH:20]=2)=O)=[CH:11][CH:10]=[CH:9][N:8]=1)C.O.[OH-].[K+]>C(O)CO.CO>[Br:21][C:18]1[O:17][C:16]([C:14]2[N:6]([CH2:5][C:4]([OH:3])=[O:22])[C:7]3=[N:8][CH:9]=[CH:10][CH:11]=[C:12]3[N:13]=2)=[CH:20][CH:19]=1Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 2
Procedure
A solution of N-[3-[(5-bromo-2-furanylcarbonyl)amino]-2-pyridinyl]glycine ethyl ester (110 g, 0.30 mole) in ethylene glycol (510 ml) was refluxed under nitrogen for two hours. The solution was cooled to room temperature and water (100 ml) and potassium hydroxide pellets (23.25 g, 0.41 mole) were added. The solution was refluxed for an additional 1.5 hours and then filtered, while hot, into ice water (2 liters). A 3N hydrochloric acid solution was added until the suspension was acidic. After stirring overnight, the solid was collected by filtration and rinsed with water. Most of the wet material was dried at 56° C. overnight under high vacuum to give 79.5 g of crude material (82%) yield). A portion (3.0 g of wet material) was dissolved in hot methanol, filtered, and cooled to room temperature. Addition of water caused a solid to precipitate which was collected by filtration, rinsed with water, and dried at high vacuum at 56° C. to give 1.59 g of title compound, mp 229°-231° C.
Workup
- temperatureThe solution was refluxed for an additional 1.5 hours
- filtrationfiltered
- additionA 3N hydrochloric acid solution was added until the suspension
- filtrationthe solid was collected by filtration
- washrinsed with water
- customMost of the wet material was dried at 56° C. overnight under high vacuum
- customto give 79.5 g of crude material (82%)
- customyield)
- filtrationfiltered
- temperaturecooled to room temperature
- additionAddition of water
- customto precipitate which
- filtrationwas collected by filtration
- washrinsed with water
- customdried at high vacuum at 56° C.
Sources & evidence
- ORD record
- ord-928aca0c22614ef6991cff8398ca056a
- Source dataset
- uspto-grants-1989_10
- Patent number
- US04873251
Reaction notes
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