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HRID 10712作成日:2026年10月26日

4-Acetylbenzenesulphonamide → HCID 178419020、化合物

https://huagongshe.com/reaction/10712

反応式

関与物質

役割名称HCID仕込み量
反応物4-AcetylbenzenesulphonamideHCID 74065—
反応物HCID 178418753HCID 178418753—
生成物HCID 178419020HCID 17841902060%

反応手順

The title compound was prepared by condensing 4-acetyl-benzenesulfonamide (Ex-26A) and 4-methoxy-2-(1H-tetrazol-5-ylmethoxy)-5-thiophen-2-yl-benzaldehyde (Ex-89A) in a similar manner as described in Ex-22. Yellow solid, mp 163–164° C. (dec), 60% yield. 1H-NMR (300 MHz, DMSO-d6) δ 8.31–8.34 (m, 3H), 7.92–8.15 (m, 4H), 7.70 (d, 1H, J=4.0 Hz), 7.54 (m, 3H), 7.15–7.17 (m, 1H), 6.92 (s, 1H), 4.64 (brs, 2H), 4.03 (s, 5H). MS (ESI) m/z=498 ([M+H]+, 100%). Anal. Calcd. for C22H19N5O5S2.1½H2O: C, 50.37; H, 4.23; N, 13.35; S, 12.23. Found: C, 50.48; H, 4.24; N, 12.95; S, 12.35.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07094801B2
出典データセットuspto-grants-2006_08
ORD IDord-6fd8cc18eef045a9bc2899c48626f66d
出典メモuspto-grants-2006_08