Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1459600생성일: 2026년 10월 26일
Water → (2S,3S)-(6-Methoxy-2-phenyl-benzothiazol-5-ylmethyl)-(2-phenyl-piperidin-3-yl)-amine
https://huagongshe.com/reaction/1459600
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Water | HCID 962 | — |
| 반응물 | Sodium triacetoxyborohydride | HCID 5049666 | — |
| 반응물 | (2S,3S)-2-phenylpiperidin-3-amine | HCID 9812908 | — |
| 반응물 | 6-Methoxy-2-phenyl-benzothiazol-5-aldehyde | HCID 22620064 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | (2S,3S)-(6-Methoxy-2-phenyl-benzothiazol-5-ylmethyl)-(2-phenyl-piperidin-3-yl)-amine | HCID 53769590 | 80% |
반응 단계
A round bottom flask equipped with a Dean Stark water separator and condenser was charged with 0.96 grams (3.6 mmol) 6-methoxy-2-phenyl-benzothiazol-5-aldehyde and 0.57 grams (3.2 mmol) of (2S, 3S)-2-phenyl-3-amino-piperidine in 90 mL of hours. The reaction mixture was evaporated in vacuo and the residue was redissolved in 90 mL of 1,2-dichlorethane. The solution was treated with 0.89 grams (4.2 mmol) of sodium triacetoxyborohydride and was stirred for 16 hours at room temperature. The reaction mixture was diluted with methylene chloride (600 mL) and washed with 150 mL of bicarbonate solution, 150 mL of water and finally with 150 mL of saturated brine solution. The organic phase was dried over sodium sulfate, filtered and evaporated. The residue was chromatographed on silica gel eluting with 97/2/1 methylene chloride, methanol, conc. aqueous ammonium hydroxide solution. Product containing fractions were combined, evaporated and crystallized from hot ether--MeOH to afford 1.1 grams (80%) of the desired product.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05854262 |
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| 출처 데이터셋 | uspto-grants-1998_12 |
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| ORD ID | ord-a6522470444842b6b903ffff98b130cc |
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| 출처 메모 | uspto-grants-1998_12 |
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