참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Methanol | HCID 887 | — |
| 반응물 | Thionyl Chloride | HCID 24386 | — |
| 반응물 | 1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid | HCID 95489 | — |
| 생성물 | methyl (3S)-1,2,3,4-tetrahydroisoquinoline-3-carboxylate hydrochloride | HCID 2760578 | — |
반응 단계
In succession 5 g of tetrahydroisoquinoline 3-carboxylic acid and 30 ml of methanol are introduced into a three-necked flask. 6 g of thionyl chloride are added to this suspension by pouring carefully, taking care that the temperature does not exceed 0, +5°. The addition takes approximately 10 minutes. After the addition is completed, stirring is continued for 2 hours at room temperature, and then the mixture is heated to reflux for 11/2 hours. Once the mixture has dissolved completely, heating is discontinued and the mixture is then evaporated to dryness. The residue is taken up three times in methanol and then evaporated to dryness. Finally, 8 g of colourless crystals are obtained and purified by trituration with ether. The crystals are separated off by filtration, washed with ether and dried. 6.4 g of methyl tetrahydroisoquinoline-3-carboxylate hydrochloride are thus obtained.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04644008 |
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| 출처 데이터셋 | uspto-grants-1987_02 |
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| ORD ID | ord-f6519eaa5551445a8f560472842abe6d |
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| 출처 메모 | uspto-grants-1987_02 |
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