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HRID 1484465作成日:2026年10月26日

1H-Indole-5-sulfonamide → HCID 178464642、化合物

https://huagongshe.com/reaction/1484465

反応式

関与物質

役割名称HCID仕込み量
反応物1H-Indole-5-sulfonamideHCID 21683100—
反応物N-ethyl-2,3-diaza-spiro[4.4]non-3-ene-2-carboximidothioic acid methyl esterHCID 53354231—
溶媒AcetonitrileHCID 6342—
生成物HCID 178464642HCID 17846464287%

反応手順

100 mg (1 mol equiv.) N-Ethyl-2,3-diaza-spiro[4.4]non-3-ene-2-carboximidothioic acid methyl ester and 92.5 mg (1.05 mol equiv.) 1H-indole-5-sulfonic acid amide were added to 3 mL acetonitrile. The reaction mixture was refluxed overnight and volatiles were removed under reduced pressure. The residue was taken up in ethyl acetate and extracted with 2N NaOH. The organic layer was dried over Na2SO4, filtered and evaporated to dryness. Purification by flash chromatography on silica gel (Et2O:EtOAc=1:1) afforded 152 mg (87%) 1H-indole-5-sulfonic acid (2,3-diaza-spiro[4.4]non-3-en-2-yl)-ethylamino-methyleneamide. 1H NMR (400 MHz, CDCl3) δ 1.14 (t, J=7.2 Hz, 3H), 1.59-1.79 (m, 8H), 3.43-3.51 (m, 2H), 3.79 (br.s., 2H), 6.63-6.65 (m, 1H), 6.76 (s, 1H), 6.99 (br.s., 1H), 7.30 (t, J=2.8 Hz, 1H), 7.43 (d, J=8.6 Hz, 1H), 7.76 (dd, J=8.6, 1.8 Hz, 1H), 8.27 (br.s., 1H), 8.54 (br.s., 1H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09422244B2
出典データセットuspto-grants-2016_08
ORD IDord-8a2f8b2419a246669fe99ede3e634c33
出典メモuspto-grants-2016_08