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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2198075Generated: October 30, 2026

Potassium Carbonate → HCID 57757976, compound

https://huagongshe.com/reaction/2198075

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantTosylmethyl isocyanideHCID 161915—
ReactantHCID 57757971HCID 57757971—
SolventMethanolHCID 887—
ProductHCID 57757976HCID 5775797639.4%

Reaction Steps

To a solution of 4-amino-5-(4-nitrophenyl)pyrrolo[2,1-f][1,2,4]triazine-6-carbaldehyde (Intermediate H, Step 2) (692 mg, 2.44 mmol) was added tosylmethyl isocyanide (477 mg, 2.44 mmol) and potassium carbonate (338 mg, 2.44 mmol) in MeOH. The solution was allowed to stir at reflux overnight. The solution was dried and diluted with EtOAc (50 mL) and THF (50 mL). Water (50 mL) was added to the reaction mixture. The solution was transferred to a separatory funnel, and the organic layer was isolated and washed with brine (50 mL). The aqueous layers were back extracted with EtOAc (2×50 mL). The combined organic layers were collected, dried (Na2SO4), concentrated onto silica gel, and purified by column chromatography (100% CH2Cl2 ramping to 95:5 v/v CH2Cl2-EtOAc) to afford 310 mg of the above compound as an yellow solid (yield 39%). 1H-NMR (DMSO-d6) δ 11.70 (s, 1H), 8.31 (d, J=8.5 Hz, 2H), 8.28 (s, 1H), 8.17 (s, 1H), 7.66 (d, J=7.1 Hz, 2H), 6.75 (s, 1H); MS [M+H]+=323.2; LCMS RT=2.57 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08338595B2
Source datasetuspto-grants-2012_12
ORD IDord-73b1d089b1b74774b374b1703ac85a7e
Source noteuspto-grants-2012_12