Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 36912생성일: 2026년 10월 25일
Methylamine → 2-(2,5-Dimethylthien-3-yl)-N-methylimidazo[2,1-b]-benzothiazole-3-acetamide
https://huagongshe.com/reaction/36912
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Methylamine | HCID 6329 | — |
| 반응물 | 2-(2,5-Dimethylthien-3-yl)imidazo[2,1-b]benzothiazole-3-acetic acid | HCID 19936706 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 2-(2,5-Dimethylthien-3-yl)-N-methylimidazo[2,1-b]-benzothiazole-3-acetamide | HCID 19936724 | — |
반응 단계
A solution of 1.5 g (0.0044 mole) of 2-(2,5-dimethylthien-3-yl)imidazo[2,1-b]benzothiazole-3-acetic acid in 30 ml of anhydrous tetrahydrofuran is treated, at room temperature, with 0.85 g (0.005 mole) of N,N'-carbonyldiimidazole for 30 minutes. The solution which has become clear is cooled to 0° C. and a stream of methylamine is passed through it for 30 minutes. The mixture is allowed to return to room temperature, the stirring is continued for 3 h, the solvent is evaporated under reduced pressure, the residue is taken up in 10 ml of water, it is extracted with dichloromethane, the organic phase is separated, it is washed with water, it is dried over sodium sulphate, the solvent is evaporated under reduced pressure, and the residue is crystallized from ethyl acetate. 1 g of pale yellow crystals is finally obtained. Melting point: 238°-239° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05418248 |
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| 출처 데이터셋 | uspto-grants-1995_05 |
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| ORD ID | ord-7156c0337bdd40d492d7eeed097f1fac |
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| 출처 메모 | uspto-grants-1995_05 |
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