Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1695293Generated: October 30, 2026

1,1'-Carbonyldiimidazole → HCID 11591381, compound

https://huagongshe.com/reaction/1695293

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantCyclopropylamineHCID 69828—
ReactantHCID 11606047HCID 11606047—
SolventDimethylformamideHCID 6228—
ProductHCID 11591381HCID 11591381—

Reaction Steps

1,1′-Carbonyldiimidazole (0.172 g, 11 mmol) was added at 25° C., to a stirred solution of compound of Example 18 (0.3 g, 7 mmol) in dry DMF (10 mL) under nitrogen atmosphere. The reaction mixture was stirred for 2 h, and cyclopropyl amine (0.06 mL, 8.4 mmol) was added. The reaction mixture was stirred at 25° C. for 2 h. Solvent was partially removed and the reaction mixture was diluted with water (50 mL), The solid separated was filtered, washed with water and dried. The product was converted to its hydrochloride salt using methanolic-HCl to obtain the title compound. Yield: 0.15 g (42.5%); 1H NMR (DMSO-d6, 300 MHz): δ 0.56 (s, 2H, CH2), 0.66 (d, 2H, CH2), 2.61 (s, 3H, CH3), 2.82 (bs, 1H, CH), 3.20-3.36 (m, 8H, 4CH2), 5.11 (s, 2H, CH2), 7.14 (d, 1H, Ar), 7.66 (d, 1H, Ar), 8.01 (s, 1H, Ar), 8.13 (s, 1H, Ar), 8.67 (s, 1H, NH); MS: m/e (ES+) 462 (M+1, freebase).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163730B2
Source datasetuspto-grants-2012_04
ORD IDord-603db74663cd42ca82f95cac203c7255
Source noteuspto-grants-2012_04