참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | 1-(4-Chlorophenoxy)acetone | HCID 239874 | — |
| 반응물 | (4-(Methylsulfanyl)phenyl)hydrazine hydrochloride | HCID 2760977 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | 3-(4-chlorophenoxy)-2-methyl-5-(methylthio)-1H-indole | HCID 68617147 | — |
반응 단계
1-(4-Chloro-phenoxy)-propan-2-one (2.66 g) was added to a stirred solution of [4-(methylthio)phenyl]-hydrazine hydrochloride (2.5 g) in MeCN (15 ml)/HCl (0.5M, 15 ml) at RT. The reaction was stirred at 50° C. for 1 h. After cooling to room temperature, the reaction was partitioned between ethylacetate/water, the organics were separated, washed with aq sodium hydroxide (1 M), dried and evaporated under reduced pressure. The residue was purified by chromatography on silica eluting with 5-20% ethylacetate/iso-hexane. The resulting hydrazone was dissolved in THF (80 ml). Sodium bicarbionate solid (1.04 g) was added followed by phosphorus trichloride (0.41 ml) dropwise, and the reaction stirred at RT for 2 h. Further phosphorus trichloride (1.20 ml) was added dropwise, and the reaction stirred at RT for 16 h. The reaction was quenched with water. The mixture was extracted with ethylacetate, the organics washed with aq. sodium hydrogencarbonate, brine, dried and evaporated under reduced pressure. The residue was purified by chromatography on silica eluting with 5-10% ethylacetate/iso-hexane. Yield 0.45 g.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07709521B2 |
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| 출처 데이터셋 | uspto-grants-2010_05 |
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| ORD ID | ord-b92b96d35dcd4878af312445a5f834de |
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| 출처 메모 | uspto-grants-2010_05 |
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