Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
1(2H)-Naphthalenone, 2-bromo-3,4-dihydro- → HCID 178419874, 화합물
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 1(2H)-Naphthalenone, 2-bromo-3,4-dihydro- | HCID 101120 | — |
| 반응물 | 2-bromo-6,7,8,9-tetrahydro-5H-benzo(7)annulen-5-one | HCID 10243312 | — |
| 반응물 | HCID 21564956 | HCID 21564956 | — |
| 반응물 | HCID 178419887 | HCID 178419887 | — |
| 반응물 | HCID 178487043 | HCID 178487043 | — |
| 생성물 | HCID 178419874 | HCID 178419874 | — |
반응 단계
When an equivalent amount of 2-bromo-benzo[b]cycloheptanone or 2-bromo-8-methoxy-benzo[b]cycloheptanone is substituted for the 2-bromo-α-tetralone in step A of example 1 above, there is obtained following the processes of steps A of example 1 and B above, 3-(4-pyridyl)-2,4,5,6-tetra-hydrobenzo[6,7]-cyclohepta[1,2-c]pyrazole(m.p. 217°-219°C) or 9-methoxy-3-(4-pyridyl)-2,4,5,6-tetrahydrobenzo[6,7]cyclohepta [1,2-c]pyrazole (m.p. 200°-201°C) respectively.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US03932430 |
| 출처 데이터셋 | uspto-grants-1976_01 |
| ORD ID | ord-b0b03184590f46efab3160eabb91b793 |
| 출처 메모 | uspto-grants-1976_01 |