Hydrochloric Acid → HCID 68814780、化合物
反応式
C[O:2][C:3](=[O:22])[C:4]1[CH:16]=[C:15](C(=O)C(C)C)[CH:14]=[C:6]([C:7]([N:9]([CH3:13])[CH2:10][CH2:11][CH3:12])=[O:8])[CH:5]=1.[OH-:23].[Na+].Cl>CO>[C:3]([C:5]1[C:6]([C:7]([N:9]([CH3:13])[CH2:10][CH2:11][CH3:12])=[O:8])=[CH:14][CH:15]=[CH:16][C:4]=1[C:3]([OH:2])=[O:22])(=[O:23])[CH:4]([CH3:16])[CH3:5]参加物
5
実験手順
Dissolve 5-isobutyryl-N-methyl-N-propyl-isophthalamic acid methyl ester (50 mg, 0.16 mmol) in methanol (3 mL) and add dropwise 2 N NaOH (0.16 mL). Stir the mixture at room temperature for 6 h, store overnight at 4° C. and acidify to about pH=6 by 5 N HCl. Concentrate to near dryness and dilute the residue with ethyl acetate. Wash with saturated aqueous sodium chloride solution and extract the organic layer, dry (magnesium sulfate) and concentrate to give the title compound.
後処理
- waitstore overnight at 4° C.
- concentrationConcentrate
- additiondilute the residue with ethyl acetate
- washWash with saturated aqueous sodium chloride solution
- extractionextract the organic layer
- dry with materialdry (magnesium sulfate)
- concentrationconcentrate
出典と根拠
- ORDレコード
- ord-2eb32b244a384d9fb7c9d3798f9a92d3
- 出典データセット
- uspto-grants-2009_09
- 特許番号
- US07585885B2
反応ノート
読み込み中…