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HRID 456500作成日:2026年10月25日

Tributylphosphine → 6-Chloro-N-(3-furylmethyl)-N-{(3S)-1-[(1S)-1-methyl-2-morpholin-4-yl-2-oxoethyl]-2-oxopyrrolidin-3-yl}naphthalene-2-sulfonamide

https://huagongshe.com/reaction/456500

反応式

関与物質

役割名称HCID仕込み量
反応物TributylphosphineHCID 13831—
反応物3-FuranmethanolHCID 20449—
反応物Diisopropyl diazene-1,2-dicarboxylateHCID 75555—
反応物6-Chloro-N-{(3S)-1-[(1S)-1-methyl-2-(4-morpholinyl)-2-oxo ethyl]-2-oxo-3-pyrrolidinyl}-2-naphthalenesulfonamideHCID 6852168—
溶媒TetrahydrofuranHCID 8028—
生成物6-Chloro-N-(3-furylmethyl)-N-{(3S)-1-[(1S)-1-methyl-2-morpholin-4-yl-2-oxoethyl]-2-oxopyrrolidin-3-yl}naphthalene-2-sulfonamideHCID 10143807—

反応手順

A solution of 6-chloro-N-{(3S)-1-[(1S)-1-methyl-2-morpholin-4-yl-2-oxoethyl]-2-oxopyrrolidin-3-yl}naphthalene-2-sulfonamide [Example 1] (0.015 g) in THF (0.5 ml) was treated with diisopropyl azodicarboxylate (0.01 ml), 3-furanmethanol (0.004 ml) and tri-n-butylphosphine (0.008 ml) and shaken at room temperature for 60 h. The mixture was concentrated under reduced pressure and the residue purified by mass directed preparative h.p.l.c. to give the title compound (0.015 g) as a colourless gum.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07186717B2
出典データセットuspto-grants-2007_03
ORD IDord-3db7d668747f417cad2339a15a3fbca2
出典メモuspto-grants-2007_03