Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | K-252C | HCID 3815 | — |
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Undec-4-ene | HCID 136496 | — |
| Product | Ngic-I | HCID 3714 | — |
Reaction Steps
300 mg (0.96 mmole) 6,7,12,13-tetrahydro-5-oxo-5H-indolo[2.3-a]pyrrolo [3,4-c]carbazole, suspended in 20 mL acetonitrile, are mixed with 0.3 mL (4.56 mole) acrylic acid nitrile and 2 drops of 1,8-diazabicyclo[5,4,0[undec-7-ene (DBU) and stirred for 3 days at 20° C. The mixture of starting materials and product is filtered off, again mixed with the same amounts of acrylic acid nitrile, DBU and acetonitrile and stirred for a further 3 days at 20° C. After again repeating this procedure and after a further 3 days at 20° C., the 12-(2-cyanoethyl)-6,7,12, 13-tetrahydro-5-oxo-5H-indolo[2,3-a]pyrrolo[3,4-c]carbazole is filtered off in the form of beige colored crystals which decompose above 275° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05489608 |
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| Source dataset | uspto-grants-1996_02 |
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| ORD ID | ord-88f9310c8bde4528a8005ced7eac3c75 |
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| Source note | uspto-grants-1996_02 |
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