참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Potassium Nitrate | HCID 24434 | — |
| 반응물 | 4-Fluoroisoquinoline | HCID 640973 | — |
| 용매 | Sulfuric Acid | HCID 1118 | — |
| 생성물 | HCID 57827875 | HCID 57827875 | — |
반응 단계
Specifically, 4-fluoroisoquinoline (3) is nitrified with potassium nitrate in sulfuric acid, to thereby form 4-fluoro-5-nitroisoquinoline (4a) and a position isomer (4b) thereof [step A]. Subsequently, these two products are reduced by use of concentrated hydrochloric acid and stannous chloride dihydrate, to thereby form 4-fluoro-5-aminoisoquinoline (5a) and a position isomer (5b) thereof [step B]. 5-Amino-4-fluoroisoquinoline (5a) is separated through column chromatography for purification [step C]. The purified product is diazotized with sodium nitrite [step D]. The diazo compound is subjected to Sandmeyer reaction employing SO2 gas-saturated acetic acid and cupric chloride dihydrate [step E], to thereby yield 4-fluoroisoquinoline-5-sulfonyl chloride (2a).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07872136B2 |
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| 출처 데이터셋 | uspto-grants-2011_01 |
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| ORD ID | ord-320f6e4891724c1588cfbf934bd25e3a |
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| 출처 메모 | uspto-grants-2011_01 |
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