HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1671566Generated: October 27, 2026
Triethylamine → 4-Methyl-piperazine-1-carboxylic acid[2-((r)-indan-1-ylamino)-quinolin-5-yl]-amide
https://huagongshe.com/reaction/1671566
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | Triphosgene | HCID 94429 | — |
| Reactant | (R)-N2-Indan-1-yl-quinoline-2,5-diamine | HCID 44219082 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-Methyl-piperazine-1-carboxylic acid[2-((r)-indan-1-ylamino)-quinolin-5-yl]-amide | HCID 44219551 | 32.5% |
Reaction Steps
To a stirred solution of (R)—N2-indan-1-yl-quinoline-2,5-diamine (example 16) (138 mg, 0.5 mmol) in THF (10 ml) was added at 0° C. triethylamine (56 mg, 0.55 mmol) and triphosgen (66.7 mg, 0.23 mmol). The white suspension was heated under reflux conditions for 3 h and triethylamine (56 mg, 0.55 mmol) and 1-methylpiperazine (55 mg, 0.55 mmol) were added at room temperature. The reaction mixture was allowed to stir at 50° C. for 16 h and was extracted with dichloromethane (2×30 ml). The combined organic layers were washed with water (2×20 ml), dried (MgSO4) and evaporated. The crude product was further purified by flash chromatography on silica gel (dichloromethane/MeOH) and crystallization (diethyl ether/heptane) to yield the title compound as off-white solid (30 mg, 15%). M.p. 142° C.; MS: m/e=402.5 (M+H+)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07994324B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-41fbea46e1204f8ba594d6ac11f71493 |
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| Source note | uspto-grants-2011_08 |
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