HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1767546Generated: October 30, 2026
Dimethylformamide → 2-Methoxy-6H-pyrido[2',3':4,5]pyrrolo[2,1-a]isoindole-11-carbaldehyde
https://huagongshe.com/reaction/1767546
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 2-Methoxy-6H-pyrido[2',3':4,5]pyrrolo[2,1-a]isoindole | HCID 18378698 | — |
| Product | 2-Methoxy-6H-pyrido[2',3':4,5]pyrrolo[2,1-a]isoindole-11-carbaldehyde | HCID 18758216 | — |
Reaction Steps
Under argon and in an anhydrous medium, 291 μl (3.17 mmol) of phosphorus oxychloride are added dropwise to 6 ml of N,N-dimethylformamide maintained at 0° C.: after 15 minutes' stirring, 500 mg (2.11 mmol) of the compound obtained in Step D dissolved in 10 ml of N,N-dimethylformamide are added by transfer. The reaction mixture is stirred for 30 minutes at 0° C. and then for 2 hours at room temperature. The reaction mixture is evaporated to dryness and then taken up in water: the aqueous phase is rendered alkaline with a 6N sodium hydroxide solution and extracted several times with ethyl acetate. The combined organic phases are dried over magnesium sulphate, filtered and evaporated. After washing with a petroleum ether/diethyl ether mixture, the title compound is obtained in the form of a brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07235550B2 |
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| Source dataset | uspto-grants-2007_06 |
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| ORD ID | ord-57034cc585f44e9bb3f7030cf66f460a |
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| Source note | uspto-grants-2007_06 |
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