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HRID 1017643作成日:2026年10月25日

Methanol → N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-4-(4-acetamidophenoxy)benzamide

https://huagongshe.com/reaction/1017643

反応式

関与物質

役割名称HCID仕込み量
反応物MethanolHCID 887—
反応物Diphenyl chlorophosphateHCID 75654—
反応物(3R)-1-Azabicyclo(2.2.2)octan-3-amineHCID 719215—
反応物4-(4-acetamidophenoxy)benzoic AcidHCID 3651079—
溶媒DimethylformamideHCID 6228—
溶媒DichloromethaneHCID 6344—
生成物N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-4-(4-acetamidophenoxy)benzamideHCID 1019971939%

反応手順

TEA (130 μL, 1.0 mmol) is added to a suspension of the product of Step D (250 mg, 0.9 mmol) in CH2Cl2 (9 mL). Diphenylchlorophosphate (190 μL, 0.9 mmol) is added and the resulting solution is stirred at room temperature for 30 minutes. This solution is added to a solution of (R)-3-aminoquinuclidine (110 mg, 0.88 mmol) in DMF (1 mL). The resulting solution is stirred overnight at room temperature. MeOH is added and the mixture is poured through a column of AG50W×2 ion exchange resin (H+ form). The resin is washed with MeOH and then the product is eluted with 5% TEA in MeOH. The eluent is evaporated to dryness. The product is crystallized from CH3CN to yield the desired product (130 mg, 39%). MS for C22H25N3O3 (ESI) (M+H)+ m/z 380.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06479510B2
出典データセットuspto-grants-2002_11
ORD IDord-16cd78e5436f4f8fb843027ec0241c99
出典メモuspto-grants-2002_11