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HRID 1593908作成日:2026年10月25日

2-(Benzo[1,2,5]thiadiazole-4-sulfonylamino)-4-bromobenzoic acid → (S)-2-[2-(Benzo[1,2,5]thiadiazole-4-sulfonylamino)-4-bromo-benzoylamino]-3-(3-bromo-4-fluoro-phenyl)-propionic acid

https://huagongshe.com/reaction/1593908

反応式

関与物質

役割名称HCID仕込み量
反応物2-(Benzo[1,2,5]thiadiazole-4-sulfonylamino)-4-bromobenzoic acidHCID 16090744—
反応物(S)-2-amino-3-(3-bromo-4-fluoro-phenyl)-propionic acid methyl ester hydrochlorideHCID 68768499—
生成物(S)-2-[2-(Benzo[1,2,5]thiadiazole-4-sulfonylamino)-4-bromo-benzoylamino]-3-(3-bromo-4-fluoro-phenyl)-propionic acidHCID 45486976—

反応手順

The title compound was prepared from 3-bromo-4-fluoro-L-phenylalanine methyl ester hydrochloride and 2-(benzo[1,2,5]thiadiazole-4-sulfonylamino)-4-bromo-benzoic acid as in Example 1, Part C, followed by hydrolysis of the resulting methyl ester as in EXAMPLE 2, Part E. HPLC: RT=9.75 min. MS (ESI−): mass calcd. for C22H15Br2FN4O5S2, 658.32; m/z found, 655/657/659 [M−H]−. 1H NMR (400 MHz, acetone-d6): 11.76 (s, 1H), 8.46-8.41 (m, 1H), 8.32-8.27 (m, 1H), 8.16-8.09 (m, 1H), 7.93-7.82 (m, 2H), 7.66-7.60 (m, 1H), 7.53-7.47 (m, 1H), 7.41-7.34 (m, 1H), 7.24-7.11 (m, 2H), 4.95-4.86 (m, 1H), 3.39-3.31 (m, 1H), 3.21-3.12 (m, 1H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07297816B2
出典データセットuspto-grants-2007_11
ORD IDord-c22dde098c5447c7b9465e31ea4b5483
出典メモuspto-grants-2007_11