참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Water | HCID 962 | — |
| 반응물 | Cyclopropylamine | HCID 69828 | — |
| 반응물 | Potassium Fluoride | HCID 522689 | — |
| 반응물 | 2-Chloro-N-(2-chloro-4-methyl-3-pyridinyl)-3-pyridinecarboxamide | HCID 10423868 | — |
| 용매 | O-Xylene | HCID 7237 | — |
| 생성물 | N-(2-Chloro-4-methylpyridin-3-yl)-2-(cyclopropylamino)nicotinamide | HCID 9972204 | — |
반응 단계
2-Chloro-N-(2-chloro-4-methyl-3-pyridinyl)-3-pyridine carboxamide (100 g), potassium fluoride (22.62 g), cyclopropylamine (80.85 g) were suspended in o-xylene (300 ml) and heated to 130-140° C. in autoclave for 5-9 h. Then the reaction mass was cooled to 25-30° C., diluted with o-xylene (500 ml) and further heated the reaction mass to 70-75° C. Thereafter, DM water (300 ml) added and stirred for 10 min at 70-75° C. The aqueous layer was separated at hot condition and organic layer was washed with DM water (300 ml) at 70-75° C. and organic layer was concentrated at 60-63° C. under reduced pressure up to residue weight attained is approximately 400 g. The concentrated mass was cooled to 25-30° C. and stirred for 15 min and further cooled to 5-10° C. and stirred for 30 min. Filtered the solid obtained and washed with chilled o-xylene (100 ml, 5-10° C.). Dried the obtained solid at 50-60° C. under reduced pressure.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08212025B2 |
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| 출처 데이터셋 | uspto-grants-2012_07 |
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| ORD ID | ord-f0479f02c46f43e5a248a3daa2e0b0d5 |
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| 출처 메모 | uspto-grants-2012_07 |
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