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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1855529Generated: November 2, 2026

4-(2-Methyl-1,3-oxazol-5-yl)aniline → 2-{6-(4-Chloro-phenyl)-2-[4-(2-methyl-oxazol-5-yl)-phenylamino]-pyrimidin-4-yl}-propan-2-ol

https://huagongshe.com/reaction/1855529

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(2-Methyl-1,3-oxazol-5-yl)anilineHCID 1518774—
Reactant2-[2-Chloro-6-(4-chloro-phenyl)-pyrimidin-4-yl]-propan-2-olHCID 86656702—
Product2-{6-(4-Chloro-phenyl)-2-[4-(2-methyl-oxazol-5-yl)-phenylamino]-pyrimidin-4-yl}-propan-2-olHCID 5782980422.2%

Reaction Steps

Using in analogous manner the procedure described in example 1e), 2-[2-chloro-6-(4-chloro-phenyl)-pyrimidin-4-yl]-propan-2-ol (112 mg, 0.3 mmol) was reacted with 4-(2-methyl-oxazol-5-yl)-phenylamine (61 mg, 0.3 mmol) to give the title compound as light yellow solid (28 mg, 22%). MS ISP (m/e): 421.1 [(M+H)+]. 1H NMR (CDCl3, 300 MHz): δ (ppm)=8.04, 7.74, 7.63 and 7.50 (4 d, 4×2H), 7.20 (s, 1H), 7.23 (s, 1H), 7.15 (s, 1H), 4.01 (s, 1H), 2.53 (s, 3H), 1.61 (s, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08962834B2
Source datasetuspto-grants-2015_02
ORD IDord-3fb0814b91834b90a7730d503d9f9724
Source noteuspto-grants-2015_02