HCID 67951109、化合物 → HCID 3441859、化合物
反応式
[CH3:1][C:2]1[CH:7]=[C:6]([CH3:8])[N:5]=[C:4]2[S:9][N:10]([CH2:13][C:14]([O:16]C)=[O:15])[C:11](=[O:12])[C:3]=12>Cl.O>[CH3:1][C:2]1[CH:7]=[C:6]([CH3:8])[N:5]=[C:4]2[S:9][N:10]([CH2:13][C:14]([OH:16])=[O:15])[C:11](=[O:12])[C:3]=12参加物
4
反応条件
- 温度
- 100 °C
実験手順
Ester 7 (160 mg, 0.63 mmol) was suspended in conc. HCl (4 mL) and heated with stirring at 100° C. for 5 h until hydrolysis completed. The mixture was cooled to room temperature, diluted with water (500 mL), and the precipitate was collected to give the title compound (151 mg, 100% yield). C10H10N2O3S; white solid; mp 355° C. (decomposed); 1H NMR (400 MHz, CD3OD) δ 7.13 (1H, s), 4.60 (2H, s), 2.71 (3H, s), 2.59 (3H, s); 13C NMR (100 MHz, CD3OD) δ 170.2, 165.7, 164.2, 163.3, 151.3, 123.3, 115.1, 45.2, 24.7, 17.9; ESI-HRMS (negative mode) calcd for C10H9N2O3S: 237.0334. found: m/z 237.0329 [M−H]−.
後処理
- temperatureheated
- temperatureThe mixture was cooled to room temperature
- customthe precipitate was collected
出典と根拠
- ORDレコード
- ord-8834240423bf48b4adc71ea7a6cae657
- 出典データセット
- uspto-grants-2016_03
- 特許番号
- US09278982B2
反応ノート
読み込み中…