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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1828344Generated: October 30, 2026

Ammonia → (r)-1-Aminocarbonylmethyl-3-(5-chloroindole-2-carbonylamino)-3,4-dihydrocarbostyril

https://huagongshe.com/reaction/1828344

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
Reactant(R)-1-carbomethoxymethyl-3-(5-chloroindole-2-carbonylamino)-3,4-dihydrocarbostyrilHCID 69194658—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
Product(r)-1-Aminocarbonylmethyl-3-(5-chloroindole-2-carbonylamino)-3,4-dihydrocarbostyrilHCID 69196722—

Reaction Steps

(R)-1-carbomethoxymethyl-3-(5-chloroindole-2-carbonylamino)-3,4-dihydrocarbostyril (Example 7) (5.6 mg) was dissolved in a mixture of tetrahydrofuran (2 mL) and 2 M ammonia in methanol solution (2 mL). After stirring for 16 h at room temperature, the solvent was evaporated under vacuum and the residue was coevaporated with toluene (5 mL twice) under vacuum. Purification by reverse phase preparative HPLC provided the title compound (3.4 mg). HPLC/MS [M+H]+, 397; HPLC/MS [M+H—NH3]+, 380.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07057046B2
Source datasetuspto-grants-2006_06
ORD IDord-826a6bbde2a94df7a7bcfdc224c67a15
Source noteuspto-grants-2006_06