HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1685132Generated: November 1, 2026
Diisopropylethylamine → HCID 86651928, compound
https://huagongshe.com/reaction/1685132
Participants
| Role | Name | HCID | Charge |
|---|
| 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 | HCID 68052599 | HCID 68052599 | — |
| Reactant | HCID 68052643 | HCID 68052643 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 86651928 | HCID 86651928 | — |
Reaction Steps
To a solution of 4-(4-methoxybenzyloxy)-1-methyl-3-(4-(6-(methylcarbamoyl)pyridin-3-yl)phenyl)-1H-pyrazole-5-carboxylic acid T-13 (304 mg, 0.64 mmol) in N,N-dimethylformamide (4 mL) were added N5,2-bis(2,4-dimethoxybenzyl)isoindoline-5,6-diamine T-04 (347 mg, 0.77 mmol), HATU (318 mg, 0.84 mmol) and diisopropylethylamine (0.34 mL, 2.0 mmol). The reaction mixture was stirred at room temperature for 2 hours. The crude product was diluted with ethyl acetate. The organic layer was washed with water and saturated brine. The organic layer was dried over sodium sulfate. Solvent was evaporated under reduced pressure. The crude product was purified by flash chromatography to afford the desired 5-(4-(5-(2-(2,4-dimethoxybenzyl)-6-(2,4-dimethoxybenzylamino)isoindolin-5-ylcarbamoyl)-4-(4-methoxybenzyloxy)-1-methyl-1H-pyrazol-3-yl)phenyl)-N-methylpicolinamide T-14 (410 mg, 0.45 mmol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08148363B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-2b5f49e88b4f48e0adbcc40789c83c07 |
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| Source note | uspto-grants-2012_04 |
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