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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-methyl-5H-pyrido[3,4-f]pyrrolo[1,2-b][1,2,5]triazepineHCID 14601947—
ReactantHCID 178418373HCID 178418373—
SolventTetrahydrofuranHCID 8028—
ProductHCID 14601949HCID 1460194948%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04996205
Source datasetuspto-grants-1991_02
ORD IDord-b24d83dbbe254bbeb6478d40547f68f1
Source noteuspto-grants-1991_02