Water → HCID 21705582, compound
Reaction equation
C([O:3][C:4](=[O:37])[CH2:5][CH2:6][N:7]([S:20]([C:23]1[CH:28]=[CH:27][C:26]([O:29][C:30]2[CH:35]=[CH:34][C:33]([F:36])=[CH:32][CH:31]=2)=[CH:25][CH:24]=1)(=[O:22])=[O:21])[C:8]1([C:16](=[O:19])[NH:17][OH:18])[CH2:14][CH:13]2[O:15][CH:10]([CH2:11][CH2:12]2)[CH2:9]1)C.C1(C)C=CC=CC=1.O.[OH-].[Na+]>ClCCl>[F:36][C:33]1[CH:32]=[CH:31][C:30]([O:29][C:26]2[CH:27]=[CH:28][C:23]([S:20]([N:7]([C:8]3([C:16](=[O:19])[NH:17][OH:18])[CH2:9][CH:10]4[O:15][CH:13]([CH2:12][CH2:11]4)[CH2:14]3)[CH2:6][CH2:5][C:4]([OH:37])=[O:3])(=[O:21])=[O:22])=[CH:24][CH:25]=2)=[CH:35][CH:34]=1Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 0 °C
Procedure
A solution of 15.1 mmoles of the product from Step G in dichloromethane is concentrated by rotary evaporation with the addition of 75 mL of toluene. This solution is treated with 75 mL of water, cooled to 0° C., and treated with 6.05 g (151 mmol, 10 equivalents) of sodium hydroxide pellets over 10 minutes with vigorous stirring. This mixture is stirred for 15 minutes at 0° C. and warmed to ambient temperature over one hour. The aqueous phase is separated, diluted with 7.5 mL of tetrahydrofuran, cooled to 0° C., and treated with 33 mL of 6N aqueous hydrochloric acid over 20 minutes. This mixture is stirred with 75 mL of ethyl acetate at 0° C. to ambient temperature, and the ethyl acetate phase is separated and washed with water. The ethyl acetate solution was concentrated to yield the title compound.
Workup
- temperaturewarmed to ambient temperature over one hour
- customThe aqueous phase is separated
- additiondiluted with 7.5 mL of tetrahydrofuran
- temperaturecooled to 0° C.
- additiontreated with 33 mL of 6N aqueous hydrochloric acid over 20 minutes
- stirringThis mixture is stirred with 75 mL of ethyl acetate at 0° C. to ambient temperature
- customthe ethyl acetate phase is separated
- washwashed with water
- concentrationThe ethyl acetate solution was concentrated
Sources & evidence
- ORD record
- ord-860517ec6f7a4921ad1cf28ee6f267ff
- Source dataset
- uspto-grants-2001_05
- Patent number
- US06229025B1
Reaction notes
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