HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 982321Generated: October 28, 2026
5-methyl-5H-pyrido[3,4-f]pyrrolo[1,2-b][1,2,5]triazepine → HCID 14601949, compound
https://huagongshe.com/reaction/982321
Participants
| Role | Name | HCID | Charge |
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| Reactant | 5-methyl-5H-pyrido[3,4-f]pyrrolo[1,2-b][1,2,5]triazepine | HCID 14601947 | — |
| Reactant | HCID 178418373 | HCID 178418373 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 14601949 | HCID 14601949 | 48% |
Reaction Steps
To 8.4 ml of a solution of methyl magnesium iodide (3.2M in diethyl ether, diluted with 10 ml tetrahydrofuran) was added a solution of 4.1 g of 5-methyl-5H-pyrido[3,4-f]pyrrolo[1,2-b][1,2,5]triazepine in 70 ml of tetrahydrofuran. After stirring at ambient temperature for 20 hours, the reaction mixture was quenched into 200 ml of an iced ammonium chloride solution and extracted with ethyl acetate (2×). The combined organics were washed with water followed by a saturated sodium chloride solution and dried over anhydrous magnesium sulfate. The crude product was preadsorbed on silica (230-400 mesh) and flash chromatographed (elution with diethyl ether) to afford a solid, recrystallization of which from toluene yielded 2.1 g (48%) of 10,11-dihydro-5,10-dimethyl-5H-pyrido[3,4-f]pyrrolo[1,2-b][1,2,5]triazepine, mp 157°-160° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04996205 |
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| Source dataset | uspto-grants-1991_02 |
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| ORD ID | ord-b24d83dbbe254bbeb6478d40547f68f1 |
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| Source note | uspto-grants-1991_02 |
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