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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 12205Generated: October 26, 2026

Methane → 6-chloro-7-(2-dimethylamino-ethylsulfanyl)-9H-beta-carbolin-8-ylamine

https://huagongshe.com/reaction/12205

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethaneHCID 297—
ReactantAmmonium ChlorideHCID 25517—
Reactant[2-(6-chloro-8-nitro-9H-beta-carbolin-7-ylsulfanyl)-ethyl]-dimethyl-amineHCID 67166181—
CatalystIronHCID 23925—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
Product6-chloro-7-(2-dimethylamino-ethylsulfanyl)-9H-beta-carbolin-8-ylamineHCID 67164517107%

Reaction Conditions

Temperature60 °C

Reaction Steps

A 50 ml round-bottom flask with a magnetic stirrer was charged with [2-(6-chloro-8-nitro-9H-β-carbolin-7-ylsulfanyl)-ethyl]-dimethyl-amine (106 mg, 0.30 mmol) in 8 ml of anhydrous ethanol. To the resulting orange mixture at RT was added 0.33 M aqueous ammonium chloride (1.95 ml, 0.64 mmol) and iron powder (540 mg, 9.67 mmol). The reaction mixture was heated to 60° C. and stirred vigorously for 20 hr. Next, the mixture was cooled to RT, diluted with ethyl acetate (20 ml) and activated charcoal (ca. 150 mg) was added. The resulting mixture was filtered through a pad of celite and the resulting filtrate concentrated to afford 103 mg of 6-chloro-7-(2-dimethylamino-ethylsulfanyl)-9H-β-carbolin-8-ylamine as a yellow solid. The crude product was used directly in the coupling step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07727985B2
Source datasetuspto-grants-2010_06
ORD IDord-6cee690533f34e0b838930aeaf183eee
Source noteuspto-grants-2010_06