HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1401085Generated: November 2, 2026
1-Benzoyl-2-isopropylhydrazine → HCID 71468733, compound
https://huagongshe.com/reaction/1401085
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Benzoyl-2-isopropylhydrazine | HCID 18869 | — |
| 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 86711430 | HCID 86711430 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 71468733 | HCID 71468733 | — |
Reaction Steps
To solution containing (E)-3-(1-(3-methylbut-2-enyl)-1H-indol-3-yl)acrylic acid (160 mg, 0.62 mmol, 1.0 equivalent), N′-isopropylbenzohydrazide (167.5 mg, 0.94 mmol, 1.5 equivalent) and HATU (357.4 mg, 0.94 mmol, 1.5 equivalent) dissolved in DMF (5.0 ml), N,N-diisopropylethylamine (DIPEA)(0.16 ml, 0.94 mmol, 1.5 equivalent) was slowly drop-wise added and stirred at room temperature for 24 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 (n-hexane:EtOAc=1:1) and dried so that yellow solid form of (E)-N′-isopropyl-N′-(3-(1-(3-methylbut-2-enyl)-1H-indol-3-yl)acryloyl)benzohydrazide was obtained. (99.8 mg, 39%).
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-c1136174a47d42db99854526539de480 |
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| Source note | uspto-grants-2014_12 |
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