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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 374804Generated: October 30, 2026

Ammonia → HCID 14994964, compound

https://huagongshe.com/reaction/374804

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantHCID 14994963HCID 14994963—
SolventEthyl AcetateHCID 8857—
ProductHCID 14994964HCID 14994964—

Reaction Conditions

Temperature100 °C

Reaction Steps

1.16 g of 2-(2-bromopropionylamino)-3-(2-chlorobenzoyl)-6-(3-butynyloxycarbonyl)-4,5,6,7-tetrahydro-thieno[2,3-C]pyridine was dissolved in 36 ml of ethyl acetate, into which ammonia gas was introduced under cooling conditions, followed by heating in a sealed tube at 100° C. After completion of the reaction, the mixture was cooled, to which 50 ml of ethyl acetate was added. The mixture was washed with 1N hydrochloric acid, after which the aqueous phase was neutralized with a sodium carbonate aqueous solution and extracted with chloroform. The resultant organic phase was dried with anhydrous magnesium sulfate. The solvent was distilled off under reduced conditions and the resultant residue was purified by the use of silica gel column chromatography (elution solvent: dichloromethane), thereby obtaining 0.36 g of the intended compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05482937
Source datasetuspto-grants-1996_01
ORD IDord-ee2b377de708446fbd73b7c071cacfb3
Source noteuspto-grants-1996_01