HCID 86745671, compound → HCID 19102849, compound
Reaction equation
C([O:3][C:4]([C:6]1[C:36](=[O:37])[C:35]([C:38]([O:40]CC)=[O:39])=[CH:34][C:9]2[N:10]([CH2:17][C:18]3[CH:23]=[CH:22][C:21]([C:24]4[C:25]([C:30]([O:32]C)=[O:31])=[CH:26][CH:27]=[CH:28][CH:29]=4)=[CH:20][CH:19]=3)[C:11]([CH2:13][CH2:14][CH2:15][CH3:16])=[N:12][C:8]=2[CH:7]=1)=[O:5])C>[OH-].[Na+].C(O)C>[C:4]([C:6]1[C:36](=[O:37])[C:35]([C:38]([OH:40])=[O:39])=[CH:34][C:9]2[N:10]([CH2:17][C:18]3[CH:23]=[CH:22][C:21]([C:24]4[C:25]([C:30]([OH:32])=[O:31])=[CH:26][CH:27]=[CH:28][CH:29]=4)=[CH:20][CH:19]=3)[C:11]([CH2:13][CH2:14][CH2:15][CH3:16])=[N:12][C:8]=2[CH:7]=1)([OH:5])=[O:3]Participants
4
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
An aliquot of the triester from Step (h) (300 mg) was hydrolyzed by stirring it in a mixture of 12 ml of 10% sodium hydroxide and 12 ml of ethanol for 6 h at 40° C. The azeotrope was distilled off, water (30 ml) was added and the resulting solution slowly acidified to pH 3 with HCl 2N. The resulting precipitated acid was isolated (mp 186, decomp.).
Workup
- distillationThe azeotrope was distilled off
- additionwater (30 ml) was added
- customThe resulting precipitated acid
- customwas isolated (mp 186, decomp.)
Sources & evidence
- ORD record
- ord-f2c61023845b4325bb9a7be422bccbee
- Source dataset
- uspto-grants-1994_01
- Patent number
- US05281615
Reaction notes
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