Lithium hydroxide, monohydrate → HCID 59497497、化合物
反応式
C[O:2][C:3](=[O:35])[CH2:4][CH2:5][N:6]1[C:10]2[CH:11]=[CH:12][CH:13]=[CH:14][C:9]=2[N:8]([CH2:15][C:16]2[C:25]3[C:20](=[CH:21][C:22]([O:26][Si](C(C)(C)C)(C)C)=[CH:23][CH:24]=3)[CH:19]=[CH:18][CH:17]=2)[C:7]1=[O:34].O.[OH-].[Li+]>C1COCC1.O>[OH:26][C:22]1[CH:21]=[C:20]2[C:25](=[CH:24][CH:23]=1)[C:16]([CH2:15][N:8]1[C:9]3[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=3[N:6]([CH2:5][CH2:4][C:3]([OH:35])=[O:2])[C:7]1=[O:34])=[CH:17][CH:18]=[CH:19]2参加物
実験手順
To a stirred solution of 3-{3-[6-(tert-Butyl-dimethyl-silanyloxy)-naphthalen-1-ylmethyl]-2-oxo-2,3-dihydro-benzimidazol-1-yl}-propionic acid methyl ester (200 mg, 0.41 mmol) in THF (7 ml) and water (1 ml) was added lithium hydroxide monohydrate (26 mg, 0.61 mmol) at ambient temperature. Upon complete consumption of the starting material the reaction was diluted with water, ethyl acetate and 6N HCl (adjusted to pH=2). The layers were separated and the aqueous phase was extracted once with ethyl acetate. The combined organics were dried (MgSO4), filtered and concentrated. The remaining residue was diluted with acetonitrile (3 ml) and allowed to stand over night. The resulting precipitated product was collected via filtration, washed with acetonitrile and dried on house vacuum to give 15 mg (10%) of the desired product. LCMS (ESMS): m/z 363.38 (M+H+).
後処理
- customUpon complete consumption of the starting material the reaction
- additionwas diluted with water, ethyl acetate and 6N HCl (adjusted to pH=2)
- customThe layers were separated
- extractionthe aqueous phase was extracted once with ethyl acetate
- dry with materialThe combined organics were dried (MgSO4)
- filtrationfiltered
- concentrationconcentrated
- additionThe remaining residue was diluted with acetonitrile (3 ml)
- waitto stand over night
- customThe resulting precipitated product
- filtrationwas collected via filtration
- washwashed with acetonitrile
- customdried on house vacuum
出典と根拠
- ORDレコード
- ord-79168486105a461290f9950fc966ecc6
- 出典データセット
- uspto-grants-2015_10
- 特許番号
- US09150556B2
反応ノート
読み込み中…