HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1900869Generated: October 30, 2026
Cyanogen Bromide → 2-Cyanoaminomethyl-5-methyl-2,3,6,7-tetrahydrofuro[2,3-f]quinoline-7-one
https://huagongshe.com/reaction/1900869
Participants
| Role | Name | HCID | Charge |
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| Reactant | Cyanogen Bromide | HCID 10476 | — |
| Reactant | 2-Aminomethyl-5-methyl-2,3,6,7-tetrahydrofuro[2,3-f]quinoline-7-one | HCID 23369567 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Cyanoaminomethyl-5-methyl-2,3,6,7-tetrahydrofuro[2,3-f]quinoline-7-one | HCID 23369846 | 38.5% |
Reaction Steps
2-Aminomethyl-5-methyl-2,3,6,7-tetrahydrofuro[2,3-f]quinoline-7-one (1.0 g, 4.34 mmol) was dissolved in tetrahydrofuran (120 ml), to which cyanogen bromide (2.76 g, 26 mmol) was added and the mixture was stirred at 40° C. for 4 hours. After completion of the reaction, the precipitated crystals were collected by filtration, and washed with water. As a result, 0.427 g of the title compound was obtained as yellow crystals (38.5%). Recrystallization from chloroform-methanol yielded the title compound as pale yellow needles (mp: 227°-230° C. (dec.)).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05576324 |
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| Source dataset | uspto-grants-1996_11 |
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| ORD ID | ord-2363675ac3f349609c479d8791810921 |
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| Source note | uspto-grants-1996_11 |
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