N,N'-Dicyclohexylurea → HCID 131714264、化合物
反応式
[CH3:1][S:2][C:3](=[S:15])[S:4][CH:5]([C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1)[C:6]([OH:8])=O.[CH2:16]([N+:20]([CH2:29][CH2:30][CH2:31][CH3:32])([CH2:25][CH2:26][CH2:27][CH3:28])[CH2:21][CH2:22][CH2:23][CH3:24])[CH2:17][CH2:18][CH3:19].[NH2:33][CH:34]1[CH2:37][N:36]([S:38]([O-:41])(=[O:40])=[O:39])[C:35]1=[O:42].C1(N=C=NC2CCCCC2)CCCCC1.C1(NC(=O)NC2CCCCC2)CCCCC1>C(#N)C>[CH2:29]([N+:20]([CH2:16][CH2:17][CH2:18][CH3:19])([CH2:21][CH2:22][CH2:23][CH3:24])[CH2:25][CH2:26][CH2:27][CH3:28])[CH2:30][CH2:31][CH3:32].[CH3:1][S:2][C:3](=[S:15])[S:4][CH:5]([C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1)[C:6]([NH:33][C@H:34]1[CH2:37][N:36]([S:38]([O-:41])(=[O:40])=[O:39])[C:35]1=[O:42])=[O:8]参加物
6
実験手順
A solution of 1.03 g of (±)-α-[[(methylthio)thioxomethyl]thio]benzeneacetic acid and 1.63 g of 3-amino-2-oxo-1-azetidinesulfonic acid, tetrabutylammonium salt (see Example 6A) in 30 ml of acetonitrile is treated with 0.8 g of dicyclohexylcarbodiimide dissolved in 10 ml of acetonitrile at -5° C. After stirring for about 16 hours the formed dicyclohexyl urea is filtered off and the mother liquor is evaporated. The remaining oily residue is chromatographed on a column of 400 g of silica (ethyl/acetate/methanol/water (8.5:1:0.5) is the eluent), yielding 1.3 g of the title compound.
後処理
- filtrationis filtered off
- customthe mother liquor is evaporated
- customThe remaining oily residue is chromatographed on a column of 400 g of silica (ethyl/acetate/methanol/water (8.5:1:0.5)
出典と根拠
- ORDレコード
- ord-7b2359e0f88941388ba976f4b66cbeab
- 出典データセット
- uspto-grants-1985_07
- 特許番号
- US04529698
反応ノート
読み込み中…