Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Trifluoroacetic acid → 2-(7-(Leucinyl)aminonaphtho[2,1-d]thiazol-2-yl)-4,5-dihydrothiazole-4-carboxylic acid
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Trifluoroacetic acid | HCID 6422 | — |
| 반응물 | Thioanisole | HCID 7520 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | D-Cysteine hydrochloride monohydrate | HCID 10176341 | — |
| 반응물 | 7-(Boc-leucinyl)aminonaphtho[2,1-d]thiazole-2-carbonitrile | HCID 117604981 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 2-(7-(Leucinyl)aminonaphtho[2,1-d]thiazol-2-yl)-4,5-dihydrothiazole-4-carboxylic acid | HCID 117604502 | — |
반응 단계
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.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US09447450B2 |
| 출처 데이터셋 | uspto-grants-2016_09 |
| ORD ID | ord-3f81971b3c1a40db94d050ff4c49361c |
| 출처 메모 | uspto-grants-2016_09 |