HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1912616Erstellt: 26. Oktober 2026
(1-(2,3-difluorobenzyl)-4-iodo-6-methyl-1H-pyrrolo[2,3-b]pyridin-5-yl)methanol → 1-(2,3-difluorobenzyl)-4-iodo-6-methyl-1H-pyrrolo[2,3-b]pyridine-5-carbaldehyde
https://huagongshe.com/reaction/1912616
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | (1-(2,3-difluorobenzyl)-4-iodo-6-methyl-1H-pyrrolo[2,3-b]pyridin-5-yl)methanol | HCID 71209443 | — |
| Edukt | HCID 178418287 | HCID 178418287 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 1-(2,3-difluorobenzyl)-4-iodo-6-methyl-1H-pyrrolo[2,3-b]pyridine-5-carbaldehyde | HCID 86675744 | 94,3% |
Reaktionsschritte
To a solution of (1-(2,3-difluorobenzyl)-4-iodo-6-methyl-1H-pyrrolo[2,3-b]pyridin-5-yl)methanol (8.75 g, 21.13 mmol) in dichloromethane (DCM) (200 mL) at 0° C. was added PCC (9.11 g, 42.3 mmol) and silica gel (6.4 g, 70% wt. of the amount of PCC) and the mixture was stirred at ambient temperature for 3 h. The mixture was filtered through silica gel washing with dichloromethane (1 L). The filtrate was concentrated to provide 1-(2,3-difluorobenzyl)-4-iodo-6-methyl-1H-pyrrolo[2,3-b]pyridine-5-carbaldehyde (9.44 g, 19.93 mmol, 94% yield) as a brownish solid. 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 2.90 (s, 3H), 5.56 (s, 2 H), 6.54 (d, J=3.71 Hz, 1 H), 6.88-7.05 (m, 2 H), 7.05-7.19 (m, 1 H), 7.30 (d, J=3.51 Hz, 1 H), 10.38 (s, 1 H); LCMS (m/z) ES+=412 (M+1).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08609653B2 |
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| Quelldatensatz | uspto-grants-2013_12 |
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| ORD ID | ord-33f6332600e44bf1a018f7c5817f73ae |
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| Quellennotiz | uspto-grants-2013_12 |
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