Methanamine, N-methoxy-, hydrochloride (1:1) → HCID 86625210、化合物
反応式
[CH3:1][N:2]([C:7]([O:9][CH2:10][C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1)=[O:8])[CH2:3][C:4]([OH:6])=O.C(N(C(C)C)CC)(C)C.O.ON1C2C=CC=CC=2N=N1.Cl.[CH3:38][NH:39][O:40][CH3:41].Cl.C(N=C=NCCCN(C)C)C.C(=O)([O-])O.[Na+]>CN(C)C=O>[CH2:10]([O:9][C:7](=[O:8])[N:2]([CH2:3][C:4]([N:39]([O:40][CH3:41])[CH3:38])=[O:6])[CH3:1])[C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1参加物
反応物 6
生成物 1
試薬・触媒・溶媒 1
実験手順
1.01 g of Z-SAR-OH (available from Kokusan Chemical Co., Ltd.), 4.72 mL of diisopropylethylamine, 1.83 g of 1-hydroxybenzotriazole monohydrate, and 1.32 g of N,O-dimethyl hydroxylamine hydrochloride were dissolved in 15 mL of N,N-dimethylformamide, then 2.6 g of 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride was added thereto under an ice-cold condition, and the mixture was stirred for 2.5 hours at room temperature. To the reaction solution was added a saturated aqueous solution of sodium hydrogen carbonate, and the solution was extracted with ethyl acetate. The resulting organic layer was washed with saturated brine, and then dried over anhydrous sodium sulfate. The insolubles were filtered, the filtrate was concentrated under reduced pressure, and the resulting residue was purified by silica gel column chromatography (eluent: hexane/ethyl acetate=1/1), to obtain 1.02 g of benzyl{2-[methoxy(methyl)amino]-2-oxoethyl}methylcarbamate [2-1] (hereinafter, referred to as the compound [2-1]) as a pale yellow oily product.
後処理
- extractionthe solution was extracted with ethyl acetate
- washThe resulting organic layer was washed with saturated brine
- dry with materialdried over anhydrous sodium sulfate
- filtrationThe insolubles were filtered
- concentrationthe filtrate was concentrated under reduced pressure
- customthe resulting residue was purified by silica gel column chromatography (eluent: hexane/ethyl acetate=1/1)
出典と根拠
- ORDレコード
- ord-ebeb14c3fed346c48efb367dce22f321
- 出典データセット
- uspto-grants-2011_07
- 特許番号
- US07977336B2
反応ノート
読み込み中…