참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Phenol | HCID 996 | — |
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | 4-Bromopyridinium chloride | HCID 88100 | — |
| 반응물 | 1-(Propylamino)-oxindole | HCID 15703628 | — |
| 생성물 | 1,3-dihydro-1-(propyl-4-pyridinylamino)-2H-indol-2-one | HCID 14994261 | 14.4% |
반응 단계
To a stirred solution of 1-(propylamino)-oxindole (10.4 g) and phenol (30.8 g), preheated to 150° C. under nitrogen, was added 4-bromopyridine hydrochloride (11.04 g) over 5 min. Heating was continued for 7 hours at which time the reaction mixture was cooled to room temperature and made basic by slow addition of dilute aqueous sodium hydroxide. The product was extracted four times with ethyl acetate and the combined organic layers back-extracted with dilute aqueous sodium hydroxide, washed with brine, and dried (K2CO3). Filtration and concentration gave the crude product. Purification via flash column chromatography (silica gel, EtOAc), preparative high performance liquid chromatography (HPLC) (silica gel, EtOAc→2% Et3N/0-7% MeOH/EtOAc), and a third column (alumina, EtOAc) followed. Recrystallization from ethyl acetate-pentane afforded 2.10 g (14%) of 1,3-dihydro-1-(propyl-4-pyridinylamino)-2H-indol-2-one, as a solid, m.p. 140°-143° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05006537 |
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| 출처 데이터셋 | uspto-grants-1991_04 |
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| ORD ID | ord-e5647d7bd11f446b87ff1d99d29f7409 |
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| 출처 메모 | uspto-grants-1991_04 |
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