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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 12214Generated: October 25, 2026

N-(6-chloro-8-nitro-9H-beta-carbolin-4-yl)-2,2,2-trifluoro-acetamide → N-(8-amino-6-chloro-9H-beta-carbolin-4-yl)-2,2,2-trifluoro-acetamide

https://huagongshe.com/reaction/12214

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(6-chloro-8-nitro-9H-beta-carbolin-4-yl)-2,2,2-trifluoro-acetamideHCID 86595094—
SolventMethanolHCID 887—
ProductN-(8-amino-6-chloro-9H-beta-carbolin-4-yl)-2,2,2-trifluoro-acetamideHCID 8659509595%

Reaction Steps

The crude N-(6-chloro-8-nitro-9H-β-carbolin-4-yl)-2,2,2-trifluoro-acetamide (130 mg, 0.36 mmol) was dissolved in 7 ml of MeOH and the reaction vessel was vacuum purged 3× with N2. Platinum (20 mg, 20% wt. on activated carbon) was added quickly, and the reaction vessel was again vacuum purged 3× with N2, followed by 3 additional vacuum purge cycles with H2. The reaction was allowed to stir under H2 at 1 atm overnight. Upon completion, the reaction vessel was purged of H2 and filtered over celite. The celite was washed several times with methanol until the filtrates were clear. The combined filtrates were concentrated to give N-(8-amino-6-chloro-9H-β-carbolin-4-yl)-2,2,2-trifluoro-acetamide as a yellow solid (112 mg, 95%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07727985B2
Source datasetuspto-grants-2010_06
ORD IDord-43960de9c44a4b3286a26c07d143e575
Source noteuspto-grants-2010_06