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HRID 1731760作成日:2026年10月25日

Acetone → Methyl 2-[2-Hydroxy-3-[N-[2-[N-(4-methylphenylsulfonyl)amino]ethyl]amino]propoxy]benzoate Oxalate

https://huagongshe.com/reaction/1731760

反応式

関与物質

役割名称HCID仕込み量
反応物AcetoneHCID 180—
反応物Oxalic AcidHCID 971—
反応物Methyl 2-(oxiran-2-ylmethoxy)benzoateHCID 279510—
反応物N-(2-Aminoethyl)-4-methylbenzenesulfonamideHCID 301318—
溶媒MethanolHCID 887—
生成物Methyl 2-[2-Hydroxy-3-[N-[2-[N-(4-methylphenylsulfonyl)amino]ethyl]amino]propoxy]benzoate OxalateHCID 13732868—

反応手順

A solution of 2.15 g of N-(2-aminoethyl)-p-toluenesulfonamide (0.1 mole) and 2.08 g of methyl 2-(2,3-epoxypropoxy)benzoate (0.01 mole) in 100 ml of methanol was stored at 25° C. for 4 hours. The methanol was then removed under reduced pressure, leaving an oil (NMR indicated only mono-alkylated product). The oil was then dissolved in 50 ml of methanol and an equimolar quantity of oxalic acid was added to the solution. 50 Ml of acetone was added, and the product crystallized upon refrigeration. The product was recrystallization from acetone/methanol (1:1) to yield 1.4 g of product which had a melting point of 165°-166° C. The elemental analysis (CHN) and NMR spectrum were consistent with the assigned structure.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04623652
出典データセットuspto-grants-1986_11
ORD IDord-56f42d917c074e938e6e5f2d16399366
出典メモuspto-grants-1986_11