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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1855457Generated: November 3, 2026

1-(2-Chloropyrimidin-4-yl)piperidin-4-ol → HCID 57829750, compound

https://huagongshe.com/reaction/1855457

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(2-Chloropyrimidin-4-yl)piperidin-4-olHCID 13340661—
Reactant3-methoxy-4-(4-methyl-1H-imidazol-1-yl)anilineHCID 45480181—
SolventDichloromethane methanolHCID 21226129—
ProductHCID 57829750HCID 57829750—

Reaction Steps

The title compound was prepared from 1-(2-chloropyrimidin-4-yl)-4-piperidinol (120 mg, 0.534 mmol) and 3-methoxy-4-(4-methyl-imidazol-1-yl)-phenylamine (109 mg, 0534 mmol) using in analogous manner the procedure described in example 43b). Obtained after trituration in dichloromethane/methanol (19:1 v/v) as a white solid (117 mg, 57%). MS ISP (m/e): 381.1 [(M+1-1)+]. 1H NMR (DMSO-D6, 300 MHz): δ (ppm)=9.24 (s, 1H), 7.97 (d, 1H), 7.84 (d, 1H), 7.63 (s, 1H), 7.26 (dd, 1H), 7.18 (d, 1H), 7.03 (s, 1H), 6.31 (d, 1H), 4.77 (d, 1H), 4.07 (m broad, 2H), 3.78 (s, 3H), 3.77 (m, 1H), 3.25 (m broad, 2H), 2.14 (s, 3H), 1.78 (m broad, 2H), 1.36 (m broad, 2H). Mp 197-200° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08962834B2
Source datasetuspto-grants-2015_02
ORD IDord-08b44c782b804585961948fddc9909f7
Source noteuspto-grants-2015_02