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HRID 1459600作成日:2026年10月27日

Water → (2S,3S)-(6-Methoxy-2-phenyl-benzothiazol-5-ylmethyl)-(2-phenyl-piperidin-3-yl)-amine

https://huagongshe.com/reaction/1459600

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Sodium triacetoxyborohydrideHCID 5049666—
反応物(2S,3S)-2-phenylpiperidin-3-amineHCID 9812908—
反応物6-Methoxy-2-phenyl-benzothiazol-5-aldehydeHCID 22620064—
溶媒DichloromethaneHCID 6344—
生成物(2S,3S)-(6-Methoxy-2-phenyl-benzothiazol-5-ylmethyl)-(2-phenyl-piperidin-3-yl)-amineHCID 5376959080%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05854262
出典データセットuspto-grants-1998_12
ORD IDord-a6522470444842b6b903ffff98b130cc
出典メモuspto-grants-1998_12