참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 1,2-Dichloroethane | HCID 11 | — |
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | Dihydro-3(2H)-thiophenone | HCID 61252 | — |
| 반응물 | 2-Aminobenzonitrile | HCID 72913 | — |
| 촉매 | Zincchloride | HCID 3007855 | — |
| 용매 | Methyl Ethyl Ketone | HCID 6569 | — |
| 생성물 | 2,3-Dihydrothieno[3,2-b]quinolin-9-amine | HCID 14372828 | 31.8% |
반응 단계
Anthranilonitrile (4.80 g) and tetrahydrothiophen-3-one (8.17 g) were stirred until a homogeneous mixture was obtained and then freshly fused ZnCl2 (8.0 g) was added and the reaction mixture heated at 120°. After 2 hours, 30 ml of 1,2-dichloroethane was added and the reaction mixture refluxed for an additional 2 hours. At the end of this time the reaction mixture was distributed between 10% NaOH solution and 2-butanone, after which the organic phase was separated, dried, concentrated and purified by flash chromatography (5% i-PrOH/CH2Cl2). Combination of the product-containing fractions gave 2.61 g of product that was pure to thin layer chromatography. This product was combined with that obtained in another run and recrystallized from EtOAc to give analytically pure material, mp 210°-212°.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05208330 |
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| 출처 데이터셋 | uspto-grants-1993_05 |
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| ORD ID | ord-95466a2915a543f5bae252fcc77eb8e9 |
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| 출처 메모 | uspto-grants-1993_05 |
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