Sodium Hydroxide → HCID 131719857, compound
Reaction equation
[C:1]1([CH2:7][O:8][C:9]([N:11]2[CH2:16][CH2:15][N:14]([C:17]([C@@H:19]3[O:27][CH2:26][C@H:21]([S:22]C(=O)C)[CH2:20]3)=[O:18])[CH2:13][CH2:12]2)=[O:10])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[OH-].[Na+]>CO>[C:1]1([CH2:7][O:8][C:9]([N:11]2[CH2:16][CH2:15][N:14]([C:17]([C@@H:19]3[O:27][CH2:26][C@H:21]([SH:22])[CH2:20]3)=[O:18])[CH2:13][CH2:12]2)=[O:10])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1Participants
4
Procedure
A 0° C. solution, under argon, of 0.20 g of product from Example 152 in 1.5 ml of dry methyl alcohol is treated with 0.25 ml of 4N sodium hydroxide. The reaction is monitored by thin layer chromatography. After 1 hour an additional 0.17 ml of 4N sodium hydroxide is added and the reaction stirred 1 hour. The reaction mixture is quenched with 1.86N hydrochloric acid/isopropyl alcohol, concentrated in vacuo and chromatographed (silica gel: 20-80% ethyl acetate/hexane) to give 0.116 g of the desired product.
Workup
- customThe reaction mixture is quenched with 1.86N hydrochloric acid/isopropyl alcohol
- concentrationconcentrated in vacuo
- customchromatographed (silica gel: 20-80% ethyl acetate/hexane)
Sources & evidence
- ORD record
- ord-9116bf91423b4ba78053b9e88cfa024e
- Source dataset
- uspto-grants-1997_02
- Patent number
- US05602118
Reaction notes
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