HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1401095Generated: November 1, 2026
Diisopropylethylamine → HCID 86711440, compound
https://huagongshe.com/reaction/1401095
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 86711429 | HCID 86711429 | — |
| Reactant | HCID 86711441 | HCID 86711441 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 86711440 | HCID 86711440 | — |
Reaction Steps
To solution containing 3-(1-(tert-butoxycarbonyl)-6-fluoro-1H-indol-3-yl)acrylic acid (200.0 mg, 0.66 mmol), 3-fluoro-N′-isopropylbenzohydrazide (192.8 mg, 0.98 mmol) and HATU (376.6 mg, 0.98 mmol) dissolved in DMF (5.0 ml), N,N-diisopropylethylamine (DIPEA)(0.16 ml, 0.98 mmol) was slowly drop-wise added and stirred at room temperature for 12 hr. The reaction mixture was diluted with EtOAc, washed with water and brine, dried with anhydrous MgSO4, filtered, and concentrated under reduced pressure. The residue was separated through silica gel chromatography (50% EtOAc) for refinment and dried so that white (E)-tert-butyl 6-fluoro-3-(3-(2-(3-fluorobenzoyl)-1-isopropylhydrazinyl)-3-oxoprop-1-enyl)-1H-indole-1-carboxylate was obtained (180.0 mg, 56.4%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08906952B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-2799ed15d0f14b3d902990a4e0d63f89 |
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| Source note | uspto-grants-2014_12 |
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