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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1384803Generated: November 1, 2026

Sodium borohydride → HCID 21183722, compound

https://huagongshe.com/reaction/1384803

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 21183743HCID 21183743—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 21183722HCID 2118372278.4%

Reaction Steps

5.1 g (135 mmol) of sodium borohydride are added, in several portions and at room temperature, to a solution of 10 g (27.3 mmol) of methyl 5-ethyl-8-fluoro-4-oxo-3-phenyl-3,5-dihydro-4H-pyridazino[4,5-b]indole-1-carboxylate in 200 ml of tetrahydrofuran and 5.8 ml of methanol and the mixture is stirred for 4 h at reflux. The mixture is poured onto an ice-cold 0.1N hydrochloric acid solution, an insoluble material is separated by filtration, the insoluble material being washed with water and with diethyl ether, on sintered glass, and then it is dried. 7.2 g (21.4 mmol) of compound are isolated in the form of a white solid which is used as is in the following stage.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06262045B1
Source datasetuspto-grants-2001_07
ORD IDord-6935628ff86a4ac482c33753fca9d7be
Source noteuspto-grants-2001_07