Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 704580생성일: 2026년 10월 24일
Aluminum;lithium;tetrachloride → (+/-)-6-[(3,6-Dihydro-4-phenyl-1(2H)-pyridinyl)methyl]-4,5,6,7-tetrahydro-2-benzothiazolamine
https://huagongshe.com/ko/reaction/704580
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Aluminum;lithium;tetrachloride | HCID 166981 | — |
| 반응물 | Aluminum(III) Chloride | HCID 6451240 | — |
| 반응물 | (+/-)-1-[(2-Amino-4,5,6,7-tetrahydro-6-benzothiazolyl)-carbonyl]-1,2,3,6-tetrahydro-4-phenylpyridine | HCID 15101105 | — |
| 용매 | Diethyl Ether | HCID 3283 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | (+/-)-6-[(3,6-Dihydro-4-phenyl-1(2H)-pyridinyl)methyl]-4,5,6,7-tetrahydro-2-benzothiazolamine | HCID 15101109 | — |
반응 단계
An ice-cold solution of aluminum chloride (0.80 g) in 20 ml of diethyl ether is added dropwise to a suspension of lithium aluminum chloride (0.65 g) in 30 ml of tetrahydrofuran and 30 ml of diethyl ether under nitrogen. The mixture is stirred at room temperature for 15 minutes and a solution of (±)-1-[(2-amino-4,5,6,7-tetrahydro-6-benzothiazolyl)-carbonyl]-1,2,3,6-tetrahydro-4-phenylpyridine (3.5 g) (Example 6a) in 50 ml of tetrahydrofuran is added dropwise. The reaction mixture is stirred at 40° C. for 30 minutes. After cooling in an ice bath, the reaction is quenched by careful addition of 4 ml of a 10% solution of hydrochloric acid, 4 ml of a 30% solution of sodium hydroxide and 4 ml of water. The salts that precipitate are filtered through Celite and the filtrate evaporated and purified by MPLC (silica; 5% methanol, 95% dichloromethane). The title compound is obtained as a beige solid; mp 187° -190° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04988699 |
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| 출처 데이터셋 | uspto-grants-1991_01 |
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| ORD ID | ord-151d200451404f31b9ba084a84df4a28 |
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| 출처 메모 | uspto-grants-1991_01 |
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