참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Dimethyl-p-toluidine | HCID 7471 | — |
| 반응물 | Phosphorus oxychloride | HCID 24813 | — |
| 반응물 | HCID 178432088 | HCID 178432088 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | 6-Bromo-4-chloro-3-methanesulfonyl-2-methyl-quinoline | HCID 12001623 | 18% |
반응 단계
6-Bromo-3-methanesulfonyl-2-methyl-quinolin-4-ol (example C.1) (6 g, 19 mmol) and N,N-dimethyl-p-toluidine (5.5 mL, 38 mmol) were dissolved in toluene (60 mL) and heated under argon to reflux. The phosphorous oxychloride (1.9 mL, 20.9 mL) was added and heating at reflux continued for 6.5 h. The product precipitated spontaneously upon cooling to 20° C., the crystals were filtered off and washed with little toluene. One obtained 4.19 g (66%) of light brown crystals. Since the product is somewhat soluble in toluene, the mother liquor was extracted with 3 N HCl (2×), sat. NaCl (2×). The residue was purified by chromatography on silica gel in dichloromethane. One obtained 1.17 g (18%) of additional material. MS: m/z=333/335 (M).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07728142B2 |
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| 출처 데이터셋 | uspto-grants-2010_06 |
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| ORD ID | ord-85758e9ad35f4e1f90481e2fa98a2d49 |
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| 출처 메모 | uspto-grants-2010_06 |
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