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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 40655Generated: October 26, 2026

Cyclopropanecarboxaldehyde → HCID 178510350, compound

https://huagongshe.com/reaction/40655

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclopropanecarboxaldehydeHCID 123114—
ReactantSodium PyrosulfiteHCID 656671—
Reactant5-(4-(4-Methoxybenzylamino)-5-aminopyridin-2-ylamino)pyrazine-2-carbonitrileHCID 67017474—
SolventDimethylformamideHCID 6228—
ProductHCID 178510350HCID 17851035016.1%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of crude 5-(4-(4-methoxybenzylamino)-5-aminopyridin-2-ylamino)pyrazine-2-carbonitrile (0.083 mmol), cyclopropane carboxaldehyde (5.9 mg, 0.083 mmol) and sodium metabisulfite (16 mg, 0.083 mmol) in DMF (1 mL) was heated at 100° C. for 4 hours. Upon cooling, the mixture was partitioned between ethyl acetate and water. The organic layer was washed with brine, dried (Na2SO4) and concentrated to a light brown solid. The solid was stirred at 65° C. with trifluoroacetic acid. Upon completion of the reaction, the mixture was concentrated. Preparative HPLC gave the title compound (3.7 mg, 16%). 1H NMR (d6-DMSO, 400 MHz) δ 12.60 (br s, 1H), 10.75 (br s, 1H), 8.80 (s, 1H), 8.75 (s, 1H), 8.50 (s, 1H), 8.10 (s, 1H), 2.10-2.20 (m, 1H), 1.00-1.20 (m, 4H). LCMS (2) Rt=1.68 min; m/z (ESI−) 276 (M−H); (ESI+) 278 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08530468B2
Source datasetuspto-grants-2013_09
ORD IDord-f3b59bc4629d4ec996117730bb0910e8
Source noteuspto-grants-2013_09