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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1702439Generated: October 29, 2026

Water → Pyrazolo(4,3-e)pyrido(3,2-b)(1,4)diazepin-10(1H)-one, 4,9-dihydro-1,3,9-trimethyl-

https://huagongshe.com/reaction/1702439

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantPyrazolo(4,3-e)pyrido(3,2-b)(1,4)diazepin-10(1H)-one, 4,9-dihydro-1,3-dimethyl-HCID 3069939—
SolventDimethylformamideHCID 6228—
ProductPyrazolo(4,3-e)pyrido(3,2-b)(1,4)diazepin-10(1H)-one, 4,9-dihydro-1,3,9-trimethyl-HCID 3069940—

Reaction Conditions

Temperature60 °C

Reaction Steps

An amount of 5.25 gm (0.025 mol) of 1,3-dimethyl-1,4,9,10-tetrahydro-pyrazolo[4,3-e]pyrido[3,2-b][1,4]diazepin-10-one was dissolved in 25 ml of N,N-dimethylformamide and mixed with 1.2 gm of a 55% sodium hydride dispersion in mineral oil. After stirring for 2 hours at 60° C., the solution was cooled to 40° C., and 2.2 ml of methyl iodide were added dropwise. Subsequently the mixture was stirred for 3 hours at 40° C., and after addition of 50 ml of water and cooling in the ice-bath, the desired compound was obtained in crystals. The crystals were recovered by suction filtration, and the mineral oil was washed out by means of petroleum ether.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04381303
Source datasetuspto-grants-1983_04
ORD IDord-48ec64fca1f34e6c9d3739b1b6b48e44
Source noteuspto-grants-1983_04