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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1508873Generated: October 31, 2026

2-(4-Aminophenyl)-2-methylpropan-1-ol → HCID 90112112, compound

https://huagongshe.com/reaction/1508873

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(4-Aminophenyl)-2-methylpropan-1-olHCID 21904728—
Reactant4-Chloro-2-(3-chlorophenyl)-6-ethylpyrimidineHCID 43557580—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 90112112HCID 9011211288%

Reaction Steps

Following General Procedure A1, 4-chloro-2-(3-chlorophenyl)-6-ethylpyrimidine (0.075 g, 0.29 mmol) in NMP (3 mL) was reacted with 2-(4-aminophenyl)-2-methylpropan-1-ol (0.054 g, 0.33 mmol) to afford the title compound (0.066 g, 88%) as a light yellow solid. MW=381.91. 1H NMR (DMSO-d6, 500 MHz) δ 9.54 (s, 1H), 8.35-8.28 (m, 2H), 7.63 (d, J=8.6 Hz, 2H), 7.58-7.55 (m, 2H), 7.42-7.32 (m, 2H), 6.59 (s, 1H), 4.64 (t, J=5.4 Hz, 1H), 3.42 (d, J=5.4 Hz, 2H), 2.66 (q, J=7.6 Hz, 2H), 1.32-1.18 (m, 9H); APCI MS m/z 382 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221843B2
Source datasetuspto-grants-2015_12
ORD IDord-207881d6ed3349e5a2754af4f3e8cfe2
Source noteuspto-grants-2015_12