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HRID 64517作成日:2026年10月24日

Trifluoroacetic acid → 2-(7-(Leucinyl)aminonaphtho[2,1-d]thiazol-2-yl)-4,5-dihydrothiazole-4-carboxylic acid

https://huagongshe.com/ja/reaction/64517

反応式

関与物質

役割名称HCID仕込み量
反応物Trifluoroacetic acidHCID 6422—
反応物ThioanisoleHCID 7520—
反応物Potassium CarbonateHCID 11430—
反応物D-Cysteine hydrochloride monohydrateHCID 10176341—
反応物7-(Boc-leucinyl)aminonaphtho[2,1-d]thiazole-2-carbonitrileHCID 117604981—
溶媒DichloromethaneHCID 6344—
生成物2-(7-(Leucinyl)aminonaphtho[2,1-d]thiazol-2-yl)-4,5-dihydrothiazole-4-carboxylic acidHCID 117604502—

反応手順

7-(Boc-leucinyl)aminonaphtho[2,1-d]thiazole-2-carbonitrile (69 mg, 0.16 mmol) was combined with 0.5 mL of thioanisole and 1.5 mL of DCM and stirred in an ice bath. Trifluoroacetic acid (1.5 mL) was added, and the reaction monitored by HPLC. After 1 h, solvents were removed under reduced pressure, and the remaining residue triturated with ether. The resulting solid was taken up in MeCN/H2O and treated with D-cysteine hydrochloride hydrate (55 mg, 0.31 mmol) and potassium carbonate (55 mg, 0.40 mmol). After 20 min, the reaction was filtered and the product was isolated by preparative HPLC eluting with 2→50% MeCN in 0.1% formic acid. Calcd for C21H23N4O3S2 (M+H): 443.1. found 443.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09447450B2
出典データセットuspto-grants-2016_09
ORD IDord-3f81971b3c1a40db94d050ff4c49361c
出典メモuspto-grants-2016_09