반응식
C(=O)([O-])[O-].[K+].[K+].Cl.[N:8]1([C:14]2[C:18]3[CH:19]=[CH:20][CH:21]=[CH:22][C:17]=3[S:16][N:15]=2)[CH2:13][CH2:12][NH:11][CH2:10][CH2:9]1.[I-].[K+].Cl[CH2:26][CH2:27][O:28][C:29]1[CH:34]=[CH:33][C:32]([N+:35]([O-:37])=[O:36])=[CH:31][CH:30]=1>C(#N)C>[N+:35]([C:32]1[CH:33]=[CH:34][C:29]([O:28][CH2:27][CH2:26][N:11]2[CH2:12][CH2:13][N:8]([C:14]3[C:18]4[CH:19]=[CH:20][CH:21]=[CH:22][C:17]=4[S:16][N:15]=3)[CH2:9][CH2:10]2)=[CH:30][CH:31]=1)([O-:37])=[O:36]참가 물질
6
반응물 4
생성물 1
시약·촉매·용매 1
반응 조건
- 온도
- 150 °C
실험 절차
Excess dried, −325 mesh potassium carbonate (257 mg, 1.86 mmol) was diluted in 4 mL acetonitrile and 3-piperazin-1-yl-benzoisothiazole hydrochloride (395 mg, 1.55 mmol), catalytic potassium iodide, and 1(2-chloroethoxy)-4-nitrobenzene (250 mg, 1.20 mmol) were added. This mixture was sealed in a Smith microwave vial and heated on the Smith Workstation at 150° C. for 1.5 h. After cooling, the salts were filtered off and washed with acetonitrile and the filtrate was concentrated. The residue was taken up in methylene chloride and washed with water. The organic layer was dried over sodium sulfate, and concentrated to afford 530 mg of a yellow solid. Yield 89%; 92% HPLC purity at 214 nm; mp 115° C.; MS (APCI): 385 [M+H]+.
후처리
- customThis mixture was sealed in a Smith microwave vial
- temperatureAfter cooling
- filtrationthe salts were filtered off
- washwashed with acetonitrile
- concentrationthe filtrate was concentrated
- washwashed with water
- dry with materialThe organic layer was dried over sodium sulfate
- concentrationconcentrated
출처 및 근거
- ORD 기록
- ord-cee48d3671df4eb092abef4a301d4b0a
- 출처 데이터셋
- uspto-grants-2006_09
- 특허 번호
- US07101886B2
연결된 노트
불러오는 중…