HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 928427Generated: November 1, 2026
Toluene → Ethyl 1-((1-methyl-1,2,3,4-tetrahydroquinolin-7-yl)methyl)-1H-pyrazole-4-carboxylate
https://huagongshe.com/reaction/928427
Participants
| Role | Name | HCID | Charge |
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| Reactant | Toluene | HCID 1140 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | ethyl 1H-pyrazole-4-carboxylate | HCID 142179 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Diethyl azodicarboxylate | HCID 5462977 | — |
| Reactant | (1-Methyl-1,2,3,4-tetrahydroquinolin-7-yl)methanol | HCID 58081183 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl 1-((1-methyl-1,2,3,4-tetrahydroquinolin-7-yl)methyl)-1H-pyrazole-4-carboxylate | HCID 58081247 | — |
Reaction Steps
To a stirred, cooled (0° C.) solution of (1-methyl-1,2,3,4-tetrahydroquinolin-7-yl)methanol (200 mg, 0.733 mmol), ethyl 1H-pyrazole-4-carboxylate (103 mg, 0.733 mmol) and triphenylphosphine (289 mg, 1.100 mmol) in THF (10 ml) was added dropwise a 40% solution of DEAD in toluene (0.435 ml, 1.1 mmol). The reaction mixture was stirred for 2 h at 0° C., then over night at 20° C. Saturated aqueous NaHCO3 was added and the mixture was extracted with AcOEt. The organic layer was dried over MgSO4, filtered and concentrated under reduced pressure to give the title compound. The crude product was purified by preparative HPLC (Waters SunFire Prep C18 OBD 5 μm 30*100, Flow 40 mL/min, ACN: 2 min at 5%, then to 100% within 17.5 min, RT 10.00 min) to give the title compound. HPLC (Method H) Rt=2.919 min; MS (Method A) [M+H]+=300.0
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09290485B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-a9f2698a60b649c69f57f9337a2affd9 |
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| Source note | uspto-grants-2016_03 |
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