HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1098249Erstellt: 25. Oktober 2026
2-tert-butylimino-N,N-diethyl-1-methyl-1,3,2lambda5-diazaphosphinan-2-amine → 1-(1-methyl-1H-imidazol-2-yl)-4-phenoxy-1H-pyrazolo[3,4-d]pyrimidine
https://huagongshe.com/reaction/1098249
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 2-tert-butylimino-N,N-diethyl-1-methyl-1,3,2lambda5-diazaphosphinan-2-amine | HCID 19990018 | — |
| Edukt | 4,6-Diphenoxypyrimidine-5-carbaldehyde | HCID 57438655 | — |
| Edukt | 2-Hydrazinyl-1-methyl-1H-imidazole hydrochloride | HCID 57438666 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 1-(1-methyl-1H-imidazol-2-yl)-4-phenoxy-1H-pyrazolo[3,4-d]pyrimidine | HCID 57504558 | 32% |
Reaktionsschritte
2-Hydrazinyl-1-methyl-1H-imidazole hydrochloride (Intermediate AV2) (305 mg, 2.05 mmol) was added to 4,6-diphenoxypyrimidine-5-carbaldehyde (Intermediate Z2) (600 mg, 2.05 mmol) in THF (15 mL) the resulting solution was stirred at room temperature for 5 minutes. 2-tert-Butylimino-2-diethylamino-1,3-dimethyl-perhydro-1,3,2-diazaphosphorine on polystyrene (2.8 g, 6.2 mmol) was added and sealed into a microwave tube. The reaction was heated to 120° C. for 10 hours in the microwave reactor and cooled to RT. The reaction mixture was filtered and evaporated to dryness. The crude product was purified by flash silica chromatography eluting with 0 to 5% MeOH in DCM to afford the product (190 mg, 32%). 1H NMR (400 MHz, CDCl3) δ 3.59 (3H, s), 6.95 (1H, d), 7.11 (1H, d), 7.24-7.20 (2H, m), 7.32-7.26 (1H, m), 7.44 (2H, m), 8.03 (1H, s), 8.59 (1H, s); m/z (ES+) (M+H)+=293; HPLC tR=1.65 min.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08143263B2 |
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| Quelldatensatz | uspto-grants-2012_03 |
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| ORD ID | ord-aed5e06cdec8432c8ea3023610339f1b |
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| Quellennotiz | uspto-grants-2012_03 |
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