HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1931502Generated: November 2, 2026
Benzeneacetic acid, 2-fluoro- → HCID 44218725, compound
https://huagongshe.com/reaction/1931502
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzeneacetic acid, 2-fluoro- | HCID 67979 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate | HCID 2733207 | — |
| Reactant | (R)-N2-Indan-1-yl-quinoline-2,6-diamine | HCID 57860958 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 44218725 | HCID 44218725 | 33.8% |
Reaction Steps
(R)—N2-indan-1-yl-quinoline-2,6-diamine (0.05 g, 0.18 mmol), ethyldiisopropylamine (0.068 mL, 0.4 mmol), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (EDC-HCl, 0.038 mg, 0.2 mmol), 2-(1H-benzotriazole-1-yl)-1,1,3,3-tetramethyluronium tetrafluoroborate (HOBt, 0.027 mg, 0.2 mmol) and 2-fluorophenyl acetic acid (0.031 mg, 0.2 mmol) were dissolved in tetrahydrofurane (3.0 mL). The reaction mixture was stirred at ambient temperature for 3 h. Then it was diluted with water and extracted with ethyl acetate (3×). The combined organic phases were dried on sodium sulfate and evaporated. The crude product was purified by column chromatography (silica gel, heptane, ethyl acetate 4:1/1:1). The title compound (0.025 g, 33%) was obtained as an off-white solid; MS: m/e=412.6 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08188284B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-3d749968323f4a059b1bc7c7d13f6944 |
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| Source note | uspto-grants-2012_05 |
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