Iodine → HCID 939755, 화합물
반응식
[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]2[C:10]([Cl:11])=[C:9]([C:12](OC)=[O:13])[S:8][C:7]=2[CH:16]=1.CO.[NH2:19][NH2:20].II>C(OCC)(=O)C.CCCCCC>[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]2[C:10]([Cl:11])=[C:9]([C:12]([NH:19][NH2:20])=[O:13])[S:8][C:7]=2[CH:16]=1참가 물질
실험 절차
A 100 ml, round bottomed flask, reflux condenser, gas inlet and Teflon stirrer were oven dried for 12 hours at 160° C. The apparatus was rapidly assembled, flushed with dry nitrogen gas, and cooled to room temperature. The reaction flask was charged with methyl 6-methoxy-3-chlorobenzo[b]thiophene-2-carboxylate (1.50 g, 5.85 mmole), anhydrous methanol (Aldrich, 50 ml), and anhydrous hydrazine (Aldrich, 2.5 equivalents, 0.47 g, 0.45 ml, 14.61 mmole). The stirred reaction mixture was brought to reflux and the progress of the reaction monitored by TLC (Silica, 1:1 hexane:ethyl acetate, iodine and UV visualization). After 72 hours, the completed reaction was cooled to room temperature, and further cooled to 5° C. for 1 hour. The resulting solid was filtered, washed with cold methanol (2×10 ml), and dried in vacuo. This resulted in 0.856 g of the desired material, as a white amorphous powder which was used directly.
후처리
- temperatureA 100 ml, round bottomed flask, reflux condenser, gas inlet and Teflon stirrer
- customdried for 12 hours at 160° C
- customflushed with dry nitrogen gas
- customThe stirred reaction mixture
- temperatureto reflux
- customthe completed reaction
- temperaturewas cooled to room temperature
- temperaturefurther cooled to 5° C. for 1 hour
- filtrationThe resulting solid was filtered
- washwashed with cold methanol (2×10 ml)
- customdried in vacuo
출처 및 근거
- ORD 기록
- ord-c1df27f3edd645c9beaae5186e5fccd7
- 출처 데이터셋
- uspto-grants-1999_01
- 특허 번호
- US05863936
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