戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 2201678作成日:2026年10月25日

Hydrochloric Acid → N-(2-amino-5-(thiophen-2-yl)phenyl)isobutyramide

https://huagongshe.com/reaction/2201678

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物1,4-DioxaneHCID 31275—
反応物Tert-butyl (2-isobutyramido-4-(thiophen-2-yl)phenyl)carbamateHCID 71007313—
溶媒MethanolHCID 887—
生成物N-(2-amino-5-(thiophen-2-yl)phenyl)isobutyramideHCID 8671251936%

反応手順

To a stirred solution of tert-butyl (2-isobutyramido-4-(thiophen-2-yl)phenyl)carbamate (0.2 g, 0.52 mmol) in methanol (4 mL) was added 4M HCl in Dioxane (2 mL, 0.53 mmol, 1 equiv.) at 0° C. The reaction was warmed to room temperature and stirred for 2 h. After completion the reaction was concentrated under reduced pressure then basified with a saturated aqueous solution of NaHCO3. The obtained solid was filtered and dried. The crude material was purified by column chromatography (silica gel, MeOH/CH2Cl2) to afford N-(2-amino-5-(thiophen-2-yl)phenyl)isobutyramide (0.05 mg, 36% yield). ESI+ MS: m/z 261 ([M+H]+), 1H NMR (500 MHz, d6-DMSO): δ 9.10 (s, 1H0, 7.5 (s, 1H0, 7.34 (d, J=4.5 Hz, 1H), 7.23-7.19 (m, 2H), 7.05-7.03 (m, 1H0, 6.75 (d, J=8.5 hz, 1H0, 5.03 (s, 2H), 2.67-2.64 (m, 1H), 1.13 (d, J=7 Hz, 6H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09365498B2
出典データセットuspto-grants-2016_06
ORD IDord-3c7f963030f04dcfa4b7039870522207
出典メモuspto-grants-2016_06