HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2056887Erstellt: 24. Oktober 2026
Phosgene → N-(3,4-dimethylbenzyl)-N'-(3-methyl-5-isoquinolinyl)urea
https://huagongshe.com/de/reaction/2056887
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Phosgene | HCID 6371 | — |
| Edukt | Benzenemethanamine, 3,4-dimethyl- | HCID 66888 | — |
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | 3-Methylisoquinolin-5-amine | HCID 12212055 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | N-(3,4-dimethylbenzyl)-N'-(3-methyl-5-isoquinolinyl)urea | HCID 9996072 | — |
Reaktionsschritte
3,4-Dimethylbenzylamine (0.3 mL, 2.1 mmol) in toluene (11 mL) was added carefully to a 20% w/v solution of phosgene in toluene (4.5 mL). The mixture was refluxed overnight and was then concentrated in vacuo. The residue was then taken up in toluene (10 mL) and treated with DIEA (1.5 mL, 8.63 mmol) and 5-amino-3-methylisoquinoline (155 mg, 1.08 mmol). The reaction mixture was stirred at 80° for 2 h and was then cooled to room temperature. The precipitated solid was collected by filtration and was chromatographed on silica gel (97:3 CH2Cl2—CH3OH to 9:1 CH2Cl2—CH3OH, eluant gradient) to afford the desired product, A-473191. Treatment of this solid with methanolic HCl yielded the corresponding hydrochloride salt. 1H NMR (300 MHz, DMSO-d6) δ 9.16 (s, 1H), 8.59 (s, 1H), 8.24 (d, 1H, J=7.8 Hz), 7.74 (s, 1H), 7.68 (d, 1H, J=8.2 Hz), 7.50 (t, 1H, J=7.9 Hz), 7.08-7.12 (m, 3H), 6.95 (m, 1H), 4.28 (d, 2H, 5.8 Hz), 2.64 (s, 3H), 2.22 (s, 3H), 2.20 (s, 3H); MS (ESI30 ) m/z 320 (M+H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07335678B2 |
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| Quelldatensatz | uspto-grants-2008_02 |
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| ORD ID | ord-460a3a5b640040d6907e5b3c246cb8ed |
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| Quellennotiz | uspto-grants-2008_02 |
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