Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Hydrogen Sulfide → (4-[4-(2-Oxo-1,2-dihydro-quinolin-3-yl)-thiazol-2-yl]-phenyl)-carbamic acid tert-butyl ester
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Hydrogen Sulfide | HCID 402 | — |
| 반응물 | Tert-butyl 4-cyanophenylcarbamate | HCID 10130644 | — |
| 반응물 | tert-butyl N-(4-carbamothioylphenyl)carbamate | HCID 22638585 | — |
| 용매 | Methanol | HCID 887 | — |
| 용매 | Pyridine | HCID 1049 | — |
| 생성물 | (4-[4-(2-Oxo-1,2-dihydro-quinolin-3-yl)-thiazol-2-yl]-phenyl)-carbamic acid tert-butyl ester | HCID 58810140 | — |
반응 단계
A solution of 4-cyano-tert-butyloxycarbonylaniline (2.20 g, 10.0 mmol) in 20 mL of pyridine and 5 mL of TEA was purged with H2S gas for 7.0 h. Solvents were removed under vacuum. The resulting crude 4-Boc-aminobenzene-thiocarboxamide (yellow residue, 70% purity) was used directly in the next step. A solution of 4-Bocamino-benzenethiocarboxamide (205 mg, 70% pure, 0.57 mmol) and 3-(2-bromoacetyl)hydroquinolin-2-one (Example 27b, 78 mg, 0.29 mmol) in 50 mL of MeOH was heated at reflux for 4 h. After cooling to RT, the precipitates were collected by filtration to provide the title compound as an off-white solid. MS m/z: 420.2 (M+1). HRMS m/z: 420.1358 (M+H+, C23H21N3O3S Calc'd 420.1376).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US06822097B1 |
| 출처 데이터셋 | uspto-grants-2004_11 |
| ORD ID | ord-a4d0dd2b38ca416c888d782c4b7407e0 |
| 출처 메모 | uspto-grants-2004_11 |