HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 928425Generated: October 25, 2026
Methyl iodide → Methyl 1-methyl-1,2,3,4-tetrahydroquinoline-7-carboxylate
https://huagongshe.com/reaction/928425
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | Methyl 1,2,3,4-tetrahydroquinoline-7-carboxylate | HCID 16244389 | — |
| Product | Methyl 1-methyl-1,2,3,4-tetrahydroquinoline-7-carboxylate | HCID 58081325 | — |
Reaction Steps
A suspension of methyl 1,2,3,4-tetrahydroquinoline-7-carboxylate (380 mg, 1.987 mmol), Cs2CO3 (1295 mg, 3.97 mmol) and iodomethane (0.118 ml, 1.888 mmol) was stirred for 16 hours at 20° C. After that time, more iodomethane (0.118 ml, 1.888 mmol) was added and stirring was continued for 8 hours at 60° C. The reaction mixture was allowed to cool to room temperature, filtered and concentrated under reduced pressure. The crude product was purified by preparative HPLC (Macherey-Nagel Nucleosil 100-10 C18, Flow 40 mL/min, ACN: 2 min at 5%, then to 100% within 17.5 min, RT 15.52 min) to yield the title compound. HPLC (Method H) Rt=3.005 min; MS (Method A) [M+H]+=206.1
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-cbca4275af2d4135bc96a25e4dfd630c |
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| Source note | uspto-grants-2016_03 |
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