HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2045628Generated: November 1, 2026
Cyclopropanecarboxylic acid → HCID 67441699, compound
https://huagongshe.com/reaction/2045628
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyclopropanecarboxylic acid | HCID 15655 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 67441977 | HCID 67441977 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 67441699 | HCID 67441699 | 58% |
Reaction Steps
To an ice-cold mixture of methyl 2-(2-aminophenyl)-3,3-dimethyl-1,2,3,4-tetrahydroquinoline-6-carboxylate (80 mg, 0.26 mmol, 1.0 eq.), cyclopropanecarboxylic acid (33 mg, 0.34 mmol, 1.5 eq.), N,N-diisopropylethylamine (63 mg, 0.51 mmol, 2.0 eq.) in dichloromethane (4 mL) was added a solution of phosphorus oxychloride (45 mg, 0.31 mmol, 1.2 eq.). Then the reaction mixture was stirred at room temperature for 30 min. Thin layer chromatography and LC-MS indicated that the starting material was consumed completely. The reaction was quenched with 20 mL water and extracted with ethyl acetate (20 mL×2). The combined organic layers were concentrated in vacuo and the residue was purified by column chromatography on silica gel (petroleum ether/ethyl acetate=2:1) to afford 57 mg of methyl 2-(2-(cyclopropanecarboxamido)phenyl)-3,3-dimethyl-1,2,3,4-tetrahydroquinoline-6-carboxylate as a pale yellow solid; yield: 58%. MS (ESI+APCI) M+1=379.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08586747B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-07f5c9f1c9d248609ae34a845f11a4c4 |
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| Source note | uspto-grants-2013_11 |
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