HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 58656Generated: October 27, 2026
Diisopropylethylamine → 5-(2,5-Difluorobenzyl)isoxazole-3-carboxamide
https://huagongshe.com/reaction/58656
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 9886157 | — |
| Reactant | 5-(2,5-Difluorobenzyl)isoxazole-3-carboxylic acid | HCID 66832039 | — |
| Reactant | 2-(5-chloro-2-(triethylsilyl)-1H-pyrrolo[2,3-b]pyridin-3-yl)ethanamine | HCID 66832058 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-(2,5-Difluorobenzyl)isoxazole-3-carboxamide | HCID 131737018 | — |
Reaction Steps
A mixture of 2-(5-chloro-2-(triethylsilyl)-1H-pyrrolo[2,3-b]pyridin-3-yl)ethanamine (0.128 g; 0.413 mmol), 5-(2,5-difluorobenzyl)isoxazole-3-carboxylic acid intermediate 74 (0.104 g; 0.434 mmol), HATU (N,N,N′,N′-Tetramethyl-O-(7-azabenzotriazol-1-yl)uronium hexafluorophosphate) (0.165 g: 0.434 mmol) and N,N-diisopropylethylamine (0.108 mL; 0.619 mmol) in DMF (3 mL) was stirred overnight at room temperature and concentrated under reduced pressure. The crude material was dissolved in dichloromethane and the organic layer was washed with water and concentrated under reduced pressure. The crude material was purified by flash chromatography on silica gel (eluent: 1 to 10% of ethyl acetate in dichloromethane) to give 0.108 g (49%) of N-(2-(5-chloro-2-(triethylsilyl)-1H-pyrrolo[2, 3-1)]pyridin-3-yl)ethyl)-5-(2,5-difluorobenzyl)isoxazole-3-carboxamide as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09434722B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-6d00a5e5f8a64ea5a44e3dac9a734d40 |
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| Source note | uspto-grants-2016_09 |
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