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HRID 2201031作成日:2026年10月25日

tert-butyl (1S,2R)-2-(4-carbamoyl-3-(3-phenylisoxazol-5-ylamino)phenylamino)cyclohexylcarbamate → 4-((1R,2S)-2-aminocyclohexylamino)-2-(3-phenylisoxazol-5-ylamino)benzamide

https://huagongshe.com/reaction/2201031

反応式

関与物質

役割名称HCID仕込み量
反応物tert-butyl (1S,2R)-2-(4-carbamoyl-3-(3-phenylisoxazol-5-ylamino)phenylamino)cyclohexylcarbamateHCID 69284828—
溶媒Trifluoroacetic acidHCID 6422—
生成物4-((1R,2S)-2-aminocyclohexylamino)-2-(3-phenylisoxazol-5-ylamino)benzamideHCID 5733418420.9%

反応手順

Compound tert-butyl (1S,2R)-2-(4-carbamoyl-3-(3-phenylisoxazol-5-ylamino)phenylamino)cyclohexylcarbamate (6 mg) was dissolved in TFA (1 mL). After 10 min of standing, TFA removed in vacuo. The residue was purified by HPLC to give the titled compound (1 mg). MS 392.4 (M+H); UV 202.9, 294.0 nm

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09359375B2
出典データセットuspto-grants-2016_06
ORD IDord-bb99c6388cc54999a3122392c8d5cf3e
出典メモuspto-grants-2016_06