Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 4814생성일: 2026년 10월 24일
Lawesson's reagent → 2-(2-Chloroethyl)-2,3-dihydro-4-methylpyrido[3,4-f][1,4]oxazepine-5(4H)-thione monohydrochloride
https://huagongshe.com/ko/reaction/4814
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Lawesson's reagent | HCID 87949 | — |
| 반응물 | 2-(2-chloroethyl)-2,3-dihydro-4-methylpyrido[3,4-f][1,4]oxazepin-5(4H)-one | HCID 13726400 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | 2-(2-Chloroethyl)-2,3-dihydro-4-methylpyrido[3,4-f][1,4]oxazepine-5(4H)-thione monohydrochloride | HCID 13726402 | — |
반응 단계
2-(2-Chloroethyl)-2,3-dihydro-4-methylpyrido[3,4-f][1,4]oxazepin-5(4H)-one, 15 g (0.06 mole), was dissolved in 200 ml of dry toluene and 15 g (0.037 mole) of [2,4-bis (4-methoxyphenyl)-1,3,2,4-dithiaphosphetane-2,4-disulfide was added. The mixture was refluxed for 2.5 hr and the toluene solution decanted. The residue was partitioned between dilute sodium hydroxide and chloroform. The chloroform was dried and concentrated. The residue was chromatographed on a high pressure liquid chromatograph (Waters 500) using a silica column and eluting with ethyl acetate. The fraction containing material of molecular weight 257 was concentrated. The residue in isopropyl alcohol was treated with hydrogen chloride and the resulting crystals were collected. Yield of hydrochloride salt was 0.1 g (0.6%), m.p. 168°-171° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04727152 |
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| 출처 데이터셋 | uspto-grants-1988_02 |
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| ORD ID | ord-2f0a54101bda4c5984ec97659afe8d34 |
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| 출처 메모 | uspto-grants-1988_02 |
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