Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 552218Generated: October 31, 2026

Potassium Carbonate → N-(4-amino-6-chloro-9H-beta-carbolin-8-yl)-nicotinamide

https://huagongshe.com/reaction/552218

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantN-[6-chloro-4-(2,2,2-trifluoro-acetylamino)-9H-beta-carbolin-8-yl]-nicotinamideHCID 86595097—
SolventMethanolHCID 887—
ProductN-(4-amino-6-chloro-9H-beta-carbolin-8-yl)-nicotinamideHCID 1115189710%

Reaction Conditions

Temperature60 °C

Reaction Steps

N-[6-chloro-4-(2,2,2-trifluoro-acetylamino)-9H-β-carbolin-8-yl]-nicotinamide (38 mg, 0.088 mmol, 1 equiv.) was suspended in 5 ml of MeOH and a 2 ml aqueous solution of K2CO3 (121 mg, 0.92 mmol, 10 equiv.) was added thereto. The resulting clear solution was heated at 60° C. for 11 hr. After cooling to RT, fine solids precipitated that were captured by filtration and washed with 10 ml of water to give 2.78 mg (10%) of N-(4-amino-6-chloro-9H-β-carbolin-8-yl)-nicotinamide. 1H-NMR (300 MHz, DMSO-d6): δ 11.32 (s, 1H), 10.56 (s, 1H), 9.26 (s, 1H), 8.82 (d, 1), 8.42 (d, 1), 8.36 (s, 1H), 8.18 (s, 1H), 7.79 (s, 1H), 7.70 (s, 1H), 7.64 (m, 1H), 5.91 (br, 2H). Formic acid standard conditions. DAD RT=1.55 min. M+H=338.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07951801B2
Source datasetuspto-grants-2011_05
ORD IDord-c6b75418f07546ffa7a92b89730cacc1
Source noteuspto-grants-2011_05