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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 19498Generated: October 30, 2026

Cyclopropylamine → HCID 58973060, compound

https://huagongshe.com/reaction/19498

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclopropylamineHCID 69828—
ReactantHCID 58973158HCID 58973158—
SolventIsopropanolHCID 3776—
ProductHCID 58973060HCID 58973060—

Reaction Conditions

Temperature65 °C

Reaction Steps

A mixture of N-{3-[1-(6-chloro-pyrimidin-4-yl)-1H-imidazol-2-ylamino]-4-methyl-phenyl}-benzamide (2.65 g, 6.55 mmol), cyclopropylamine (8.8 mL, 124.43 mmol) in 2-propanol (30 mL) was heated at 65° C. for 16 h. The reaction mixture was then cooled down to room temperature and concentrated. The residue yellow solid was washed with water, dried under vacuum to afford the title compound. The obtained crude title compound was directly used for the next step reaction without any further purification. 1H NMR 600 MHz (DMSO-d6) δ 11.13 (bs, 1H), 10.24 (s, 1H), 8.77 (s, 1H), 8.48 (bs, 1H), 8.10 (bs, 1H), 7.98 (d, 2H, J=6.0 Hz), 7.71 (bs, 1H), 7.57 (s, 1H), 7.52 (s, 2H), 7.34 (d, 1H, J=6.6 Hz), 7.15 (d, 1H, J=6.6 Hz), 6.88 (s, 1H), 6.74 (bs, 1H), 2.61 (bs, 1H), 2.33 (s, 3H), 0.82 (s, 2H), 0.53 (s, 2H); MS m/z 426.5 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07745437B2
Source datasetuspto-grants-2010_06
ORD IDord-f2162d80bb994642b5fa07ae344b99c2
Source noteuspto-grants-2010_06