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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1863169Generated: November 1, 2026

Pyridine → HCID 20392245, compound

https://huagongshe.com/reaction/1863169

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantHCID 20392248HCID 20392248—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 20392245HCID 20392245—

Reaction Steps

A 7.8 g. portion of 4,9-dihydro-7-nitro-10H-thieno[3,4-b][1,5]benzodiazepin-10-one in a mixture of 200 ml. of pyridine and 50 ml. of methanol with 200 mg. of 10% palladium on carbon catalyst was shaken for 2 hours in a Parr hydrogenator. The catalyst was filtered and the solvents were removed under vacuum on the steam bath. The residue was dissolved in dilute hydrochloric acid, filtered, and the filtrate was made alkaline with sodium hydroxide. The crystals which form are recovered by filtration and air dried given the desired product as a brown powder, m.p. 212°-215° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04168269
Source datasetuspto-grants-1979_09
ORD IDord-08a35eb7a4ce4988ade283bf89760d71
Source noteuspto-grants-1979_09