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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1864196Generated: October 25, 2026

N-Methylaminoethanol → 2-Chloro-4-({5-[2-(methylamino)ethoxy]quinazolin-4-yl}amino)phenol

https://huagongshe.com/reaction/1864196

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-MethylaminoethanolHCID 5247031—
Reactant2-Chloro-4-[(5-fluoroquinazolin-4-yl)amino]phenolHCID 57444978—
Reactant2-Methyl-4-({5-[2-(methylamino)ethoxy]quinazolin-4-yl}amino)phenolHCID 69054007—
Product2-Chloro-4-({5-[2-(methylamino)ethoxy]quinazolin-4-yl}amino)phenolHCID 6905759096%

Reaction Steps

2-Chloro-4-[(5-fluoroquinazolin-4-yl)amino]phenol was reacted with N-methylaminoethanol using an analogous process to that described in Example 3 for the preparation of 2-methyl-4-({5-[2-(methylamino)ethoxy]quinazolin-4-yl}amino)phenol, to give 2-Chloro-4-({5-[2-(methylamino)ethoxy]quinazolin-4-yl}amino)phenol in 96% yield; NMR spectrum (DMSO-d6) 2.41 (s, 3H), 3.05 (t, 2H), 4.36 (t, 2H), 6.97 (d, 1H), 7.12 (d, 1H), 7.31 (d, 1H), 7.63 (1H, dd), 7.70 (t, 1H), 7.96 (s, 1H), 8.47 (s, 1H) 10.47 (bs, 1H); Mass spectrum MH+ 345.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07625908B2
Source datasetuspto-grants-2009_12
ORD IDord-fcbbf74f408b4a1aa969c19ee50c22e2
Source noteuspto-grants-2009_12