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HRID 2422449作成日:2026年10月26日

Benzenesulfonyl chloride, 2,4-dichloro- → 2,4-Dichloro-N-(3,5-dichloro-4-quinolin-3-ylmethyl-phenyl)-benzenesulfonamide

https://huagongshe.com/reaction/2422449

反応式

関与物質

役割名称HCID仕込み量
反応物Benzenesulfonyl chloride, 2,4-dichloro-HCID 204419—
反応物3,5-Dichloro-4-quinolin-3-ylmethyl-phenylamineHCID 18511504—
溶媒PyridineHCID 1049—
生成物2,4-Dichloro-N-(3,5-dichloro-4-quinolin-3-ylmethyl-phenyl)-benzenesulfonamideHCID 18511601—

反応手順

2,4-Dichloro-N-(3,5-dichloro-4-quinolin-3-ylmethyl-phenyl)-benzenesulfonamide was synthesized (63%) from 3,5-dichloro-4-quinolin-3-ylmethyl-phenylamine (230), 2,4-dichlorobenzenesulfonyl chloride (Maybridge) and pyridine (EM) in a similar manner as described in Examples 70-91. 1H NMR (400 MHz, DMSO-d6) δ 11.34 (br s, 1H), 8.78 (d, J=2.0 Hz, 1H), 8.13 (d, J=8.6 Hz, 1H), 7.97 (d, J=8.6 Hz, 1H), 7.93 (d, J=1.8 Hz, 1H), 7.88 (d, J=7.9 Hz, 1H), 7.80 (s, 1H), 7.73-7.68 (m, 2H), 7.58 (t, J=7.5 Hz, 1H), 7.21 (s, 2H), 4.34 (s, 2H). MS (EI): m/z 509 (M−H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07960408B2
出典データセットuspto-grants-2011_06
ORD IDord-479515d104a848cc86c07abd370e9ae8
出典メモuspto-grants-2011_06