化工社化工社 化学情報印刷レポート · 研究参考用
Trifluoroacetic acid → 2-(7-(Leucinyl)aminonaphtho[2,1-d]thiazol-2-yl)-4,5-dihydrothiazole-4-carboxylic acid
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Trifluoroacetic acid | HCID 6422 | — |
| 反応物 | Thioanisole | HCID 7520 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | D-Cysteine hydrochloride monohydrate | HCID 10176341 | — |
| 反応物 | 7-(Boc-leucinyl)aminonaphtho[2,1-d]thiazole-2-carbonitrile | HCID 117604981 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 2-(7-(Leucinyl)aminonaphtho[2,1-d]thiazol-2-yl)-4,5-dihydrothiazole-4-carboxylic acid | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US09447450B2 |
| 出典データセット | uspto-grants-2016_09 |
| ORD ID | ord-3f81971b3c1a40db94d050ff4c49361c |
| 出典メモ | uspto-grants-2016_09 |