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HRID 2220284作成日:2026年10月27日

3-{[3-Chloro-2-(2-trifluoromethyl-biphenyl-4-yl)-benzo[b]thiophen-5-ylmethyl]-amino}-propionic acid tert-butyl ester → 3-{[3-Chloro-2-(2-trifluoromethyl-biphenyl-4-yl)-benzo[b]thiophen-5-ylmethyl]-amino}-propionic acid

https://huagongshe.com/reaction/2220284

反応式

関与物質

役割名称HCID仕込み量
反応物3-{[3-Chloro-2-(2-trifluoromethyl-biphenyl-4-yl)-benzo[b]thiophen-5-ylmethyl]-amino}-propionic acid tert-butyl esterHCID 68451228—
溶媒Trifluoroacetic acid methylene chlorideHCID 21863450—
生成物3-{[3-Chloro-2-(2-trifluoromethyl-biphenyl-4-yl)-benzo[b]thiophen-5-ylmethyl]-amino}-propionic acidHCID 1128323359.4%

反応手順

3-{[3-Chloro-2-(2-trifluoromethyl-biphenyl-4-yl)-benzo[b]thiophen-5-ylmethyl]-amino}-propionic acid tert-butyl ester (43 mg, 0.079 mmol) is dissolved in TFA/CH2Cl2 (1/1) (1 mL). The solution is stirred at room temperature for an hour. The mixture is concentrated and purified by reversed phase preparative LC/MS to give 23 mg of 3-{[3-chloro-2-(2-trifluoromethyl-biphenyl-4-yl)-benzo[b]thiophen-5-ylmethyl]-amino}-propionic acid: 1H NMR (CD3OD, 400 MHz) δ 8.10 (s, 1 H), 7.96-8.02 (m, 3 H), 7.54 (d, 1 H), 7.46 (d, 1 H), 7.35-7.37 (m, 3 H), 7.28-7.29 (m, 2 H), 4.37 (s, 2 H), 3.26(m, 2 H), 2.71 (m, 2 H), MS (ES+) 490.3 (M+H+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07417065B2
出典データセットuspto-grants-2008_08
ORD IDord-b91cc9d5e9cf40d9981b245caab5b5f5
出典メモuspto-grants-2008_08