Sulfuryl chloride → N-cyclobutylsulfamoyl chloride
反応式
[S:1]([Cl:5])(Cl)(=[O:3])=[O:2].Cl.[CH:7]1([NH2:11])[CH2:10][CH2:9][CH2:8]1>CC#N>[CH:7]1([NH:11][S:1]([Cl:5])(=[O:3])=[O:2])[CH2:10][CH2:9][CH2:8]1参加物
4
実験手順
Sulfuryl chloride (104 mmol) was dissolved in dry CH3CN (25 mL), added cyclobutylamine hydrochloride (31 mmol) and stirred at reflux for 16 h. The obtained reaction mixture was cooled to rt and concentrated in vacuo. The obtained residue was trituated with Et2O (2×25 mL). The combined Et2O-phases were concentrated in vacuo affording the title compound as oil.
後処理
- temperatureat reflux for 16 h
- customThe obtained reaction mixture
- concentrationconcentrated in vacuo
- concentrationThe combined Et2O-phases were concentrated in vacuo
出典と根拠
- ORDレコード
- ord-62c3fc2be6e84f288f350fcd29fe402c
- 出典データセット
- uspto-grants-2016_01
- 特許番号
- US09233964B2
反応ノート
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