HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 586087Generated: October 30, 2026
1,8-Diazabicyclo(5.4.0)undec-7-ene → HCID 22337637, compound
https://huagongshe.com/reaction/586087
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | 4-tert-Butylbenzylamine | HCID 2735655 | — |
| Reactant | HCID 22337658 | HCID 22337658 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 22337637 | HCID 22337637 | — |
Reaction Steps
2,2,2-Trichloro-N-(7-methyl-1H-indazol-4-yl)acetamide (72 mg, 0.25 mmol), 4-tert-butylbenzylamine (55 mg, 0.34 mmol), and 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) (0.09 mL, 0.60 mmol) were combined in CH3CN (6 mL) and refluxed overnight. The mixture was allowed to cool to ambient temperature and was concentrated under reduced pressure. The residue was taken up in ethyl acetate and washed twice with saturated aqueous NH4Cl solution. The organic layer was dried (Na2SO4), filtered, and the filtrate was concentrated under reduced pressure. The residue was triturated with ethyl acetate to provide the title compound. The corresponding hydrochloride salt was prepared with methanolic HCl. 1H NMR (300 MHz, d6-DMSO) δ 12.90 (br s, 1H), 7.94 (d, J=1.3 Hz, 1H), 7.91 (s, 1H), 7.47 (m, 2H), 7.37 (m, 2H), 7.25 (m, 2H), 6.84 (t, J=5.8 Hz, 1H), 4.26 (d, J=5.7 Hz, 2H), 2.35 (s, 3H), 1.27 (s, 9H); MS (ESI+) m/z 337 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06933311B2 |
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| Source dataset | uspto-grants-2005_08 |
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| ORD ID | ord-3820c8f438b54657b9a5299f3ee33744 |
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| Source note | uspto-grants-2005_08 |
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