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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1638381Generated: November 1, 2026

5-methyl-5H-pyrido[3,4-f]pyrrolo[1,2-b][1,2,5]triazepine → 10,11-dihydro-5-methyl-10-phenyl-5H-pyrido[3,4-f]pyrrolo[1,2-b][1,2,5]triazepine

https://huagongshe.com/reaction/1638381

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-methyl-5H-pyrido[3,4-f]pyrrolo[1,2-b][1,2,5]triazepineHCID 14601947—
ReactantHCID 178418255HCID 178418255—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product10,11-dihydro-5-methyl-10-phenyl-5H-pyrido[3,4-f]pyrrolo[1,2-b][1,2,5]triazepineHCID 1460195064%

Reaction Steps

To 15 ml of a 3M solution of phenyl magnesium bromide in ether diluted with 15 ml of tetrahydrofuran was added a solution of 4.45 g of 5-methyl-5H-pyrido[3,4-f]pyrrolo[1,2-b][1,2,5]triazepine in 75 ml of tetrahydrofuran. After stirring at ambient temperature for 45 minutes, the reaction mixture was quenched into an iced ammonium chloride solution. The aqueous layer was extracted with ethyl acetate (2×), and the combined organics were washed with water followed by a saturated sodium chloride solution, dried over anhydrous magnesium sulfate, filtered and concentrated. The resultant solid was purified via flash chromatography (compound preadsorbed on silica; elution with diethyl ether) and recrystallized from toluene to yield 4.0 g (64%) of 10,11-dihydro-5-methyl-10-phenyl-5H-pyrido[3,4-f]pyrrolo[1,2-b][1,2,5]triazepine, mp 200°-203° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04879382
Source datasetuspto-grants-1989_11
ORD IDord-c05a97361b3f4765a7f7a5587661ac88
Source noteuspto-grants-1989_11