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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1936547Generated: November 3, 2026

Formamide → HCID 14590422, compound

https://huagongshe.com/reaction/1936547

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormamideHCID 713—
ReactantWaterHCID 962—
ReactantSarmazenilHCID 71231—
ReactantSodium MethoxideHCID 10942334—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 14590422HCID 14590422—

Reaction Steps

22.8 g Ethyl 7-chloro-5,6-dihydro-5-methyl-6-oxo-4H-imidazo[1,5-a][1,4]-benzodiazepine-3-carboxylate (V)were suspended under stirring and argon atmosphere in 91.2 ml 1,4-dioxane. 14.1 ml Formamide and 13.9 ml sodium methanolate were successively added to yield a clear light-orange solution, which turned to a white suspension after 10 minutes. This suspension was stirred two hours at 30° C. 200 ml deionized water were added in one portion and 1,4-dioxane was distilled off at 40° C. under reduced pressure. The remaining white suspension was stirred two hours at 0° C. and filtered. The precipitate (7-chloro-5,6-dihydro-5-methyl-6-oxo-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxamide (VI)) was washed with 50 ml deionized water three times and dried under reduced pressure for 18 hours at 80° C. Crude product: 19.43 g as a white powder. m.p.>250° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06391873B1
Source datasetuspto-grants-2002_05
ORD IDord-701193427da04e8ba5acbe27c3e3b525
Source noteuspto-grants-2002_05