Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1371109Generated: October 25, 2026

Dichloromethane → HCID 178433069, compound

https://huagongshe.com/reaction/1371109

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantPotassium CarbonateHCID 11430—
ReactantN-(2-Piperidylmethyl)-dimethylamineHCID 252484—
ReactantHCID 178432852HCID 178432852—
SolventWaterHCID 962—
ProductHCID 178433069HCID 17843306934.2%

Reaction Conditions

Temperature140 °C

Reaction Steps

To a mixture of 4-chloro-2-methyl-6-phenylpyrrolo[3,2-d]pyrimidine (Example 1(e)) (88.3 mg, 0.36 mmol) and N-(2-piperidylmethyl)-dimethylamine (Salor Chemical Company) (0.25 g, 1.72 mmol) was added a solution of K2CO3 (0.25 g, 1.60 mmol) in H2O (2.5 mL). This mixture was stirred at 140° C. in a closed-capped Wheaton vial for 2.5 h. After cooling, CH2Cl2 (10 mL) and H2O (10 mL) were added. The organic solution was removed and the aqueous solution was washed with CH2Cl2 (10 mL). The combined organic solutions were washed with saturated NaCl (15 mL), dried over MgSO4, filtered and concentrated under reduced pressure. The residue was purified by flash chromatography (3% MeOH:CHCl3 on silica gel) to give 43 mg (34%) of the title compound as a yellow oil. MS m/z: 350 (M+1), 305, 214. 1H NMR (DMSO-d6; 400 MHz): δ 1.63 (m, 6), 2.29 (s, 6), 2.40 (s, 3), 2.81 (m, 2), 3.03 (br t, 1, J=11.8), 4.53-4.63 (m, 2), 6.75 (s, 1), 7.37 (m, 1), 7.50 (t, 2, J=7.5), 7.81 (d, 2, J=7.8), 12.47 (s, 1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06583154B1
Source datasetuspto-grants-2003_06
ORD IDord-2a5f7bfa495244e3bf1b8a7b4069c183
Source noteuspto-grants-2003_06