HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1401084Generated: November 1, 2026
1-Benzoyl-2-isopropylhydrazine → HCID 71468732, compound
https://huagongshe.com/reaction/1401084
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Benzoyl-2-isopropylhydrazine | HCID 18869 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 6008084 | HCID 6008084 | — |
| Reactant | Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 9886157 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 71468732 | HCID 71468732 | — |
Reaction Steps
To solution containing (E)-3-(1-benzyl-1H-indol-3-yl)acrylic acid (30 mg, 0.14 mmol, 1.0 equivalent), N′-isopropylbenzohydrazide (28.92 mg, 0.16 mmol, 1.5 equivalent) and HATU (61.6 mg, 0.16 mmol, 1.5 equivalent) dissolved in DMF (3.0 ml), N,N-diisopropylethylamine (DIPEA)(0.03 ml, 0.16 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 white solid form of (E)-N′-(3-(1-benzyl-1H-indol-3-yl)acryloyl)-N-isopropylbenzohydrazide was obtained (40.6 mg, 86%).
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-93bd175bdb4f48d2b47ed5591be02b82 |
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| Source note | uspto-grants-2014_12 |
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