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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1855514Generated: November 3, 2026

4-Chloro-6-methyl-2-(piperidin-1-yl)pyrimidine → HCID 57829787, compound

https://huagongshe.com/reaction/1855514

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chloro-6-methyl-2-(piperidin-1-yl)pyrimidineHCID 17606447—
Reactant3-methoxy-4-(4-methyl-1H-imidazol-1-yl)anilineHCID 45480181—
ProductHCID 57829787HCID 5782978779%

Reaction Steps

The title compound was prepared from 3-methoxy-4-(4-methyl-imidazol-1-yl)-phenylamine (61 mg, 0.30 mmol) and 4-chloro-6-methyl-2-piperidin-1-yl-pyrimidine (70 mg, 0.33 mmol, example 97a) in analogous manner as described in example 90. The crude product was purified by stirring with diethyl ether. It was obtained in 79% yield as a grey solid. MS ISP (m/e): 379.3 (100) [(M+H)+]. 1H NMR (DMSO-D6, 300 MHz): δ (ppm)=9.29 (s, 1H), 7.88 (s, 1H), 7.65 (s, 1H), 7.22 (d, 1H), 7.04 (d, 1H), 7.03 (s, 1H), 5.89 (s, 1H), 3.80 (s, 3H), 3.74 (m, 4H), 2.15 (s, 3H), 2.14 (s, 3H), 1.60 (m, 2H), 1.50 (m, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08962834B2
Source datasetuspto-grants-2015_02
ORD IDord-e28ec262e95948a8ab2274b3048cbda7
Source noteuspto-grants-2015_02