反応式
[CH:1](NC(C)C)(C)C.C([Li])CCC.[O:13]=[C:14]1[O:18][CH2:17][C@H:16]([NH:19][C:20](=[O:29])[O:21][CH2:22][C:23]2[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=2)[CH2:15]1.CI.[Cl-].[NH4+]>C1COCC1.CCCCCC.C[C@H]1O[C@H]2[C@H](O)[C@@H](O)[C@H](OC3C4C(=CC5OCOC=5C=4)[C@@H](C4C=C(OC)C(O)=C(OC)C=4)[C@@H]4[C@@H]3COC4=O)O[C@@H]2CO1.C1COP(NCCCl)(=O)N(CCCl)C1.[NH2-].[NH2-].Cl[Pt+2]Cl.O>[CH3:1][C@H:15]1[C:14](=[O:13])[O:18][CH2:17][C@@H:16]1[NH:19][C:20](=[O:29])[O:21][CH2:22][C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1参加物
反応物 5
生成物 1
試薬・触媒・溶媒 4
反応条件
- 温度
- 0 °C
実験手順
272 μl (1.9 mmol) diisopropylamine are placed in 3 ml THF and while cooling with ice 1.2 ml (1.9 mmol) of an n-butyllithium solution in hexane (1.6M) are added. The mixture is stirred for 10 minutes at 0° C., then cooled to −78° C. and a solution of 200 mg (0.85 mmol) benzyl (R)-(5-oxo-tetrahydrofuran-3-yl)-carbamate in 1 ml THF is added dropwise. The mixture is stirred for one hour at −78° C. Then 210 μl (3.3 mmol) methyl iodide are added dropwise, and the mixture is heated to −60° C. within one hour. Then 0.5 ml sat. ammonium chloride solution is added and the mixture is heated to ambient temperature. Water is added and the mixture is extracted three times with ethyl acetate. The combined organic phases are dried over sodium sulphate and evaporated to dryness. The residue is taken up in DMF, acidified with TFA and purified by reversed-phase chromatography.
後処理
- temperaturecooled to −78° C.
- stirringThe mixture is stirred for one hour at −78° C
- temperaturethe mixture is heated to −60° C. within one hour
- temperaturethe mixture is heated to ambient temperature
- extractionthe mixture is extracted three times with ethyl acetate
- dry with materialThe combined organic phases are dried over sodium sulphate
- customevaporated to dryness
- custompurified by reversed-phase chromatography
出典と根拠
- ORDレコード
- ord-5b312c38ffbe4103ae25f7061656ab9e
- 出典データセット
- uspto-grants-2009_11
- 特許番号
- US07615549B2
関連ノート
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