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HRID 1453882作成日:2026年10月25日

1,2-Dichloroethane → HCID 178499181、化合物

https://huagongshe.com/reaction/1453882

反応式

関与物質

役割名称HCID仕込み量
反応物1,2-DichloroethaneHCID 11—
反応物TriethylamineHCID 8471—
反応物HOAtHCID 181649—
反応物HalostachineHCID 6950649—
反応物Methyl 4-benzyloxy-3-carboxy-1H-pyrazole-5-carboxylateHCID 57528495—
溶媒DimethylformamideHCID 6228—
生成物HCID 178499181HCID 178499181—

反応手順

To a solution of methyl 4-benzyloxy-3-carboxy-1H-pyrazole-5-carboxylate (1.5 g, 5.43 mmol; prepared as in Example 31, Step 1) in DMF (20 mL) were added HOAT (1.11 g, 8.15 mmol), (1R)-2-(methylamino)-1-phenylethanol (1.23 g, 8.15 mmol; prepared as described in Gurjar, M. K., et al., Org. Process Res. Dev. 1998, 2, 422.), triethylamine (0.82 g, 8.15 mmol), and EDC (1.56 g, 8.15 mmol). The reaction mixture was stirred at ambient temperature for 3 hours. The DMF was removed in vacuo and the residue was partitioned between saturated aqueous NH4Cl and EtOAc. The layers were separated and the aqueous was extracted twice more with EtOAc. The combined organic extracts were dried over Na2SO4 and concentrated in vacuo to afford the title product. ES MS (M+1)=410.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07476666B2
出典データセットuspto-grants-2009_01
ORD IDord-965f9976a6524d59ae52ffcd2b885b17
出典メモuspto-grants-2009_01