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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1867707Generated: November 1, 2026

Ethyl (R)-2-(trifluoromethylsulfonyloxy)propionate → N-({4-[(3-chloro-2-fluorophenyl)amino]-7-methoxyquinazolin-6-yl}methyl)-N-(2-methoxyethyl)-L-alanine

https://huagongshe.com/reaction/1867707

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl (R)-2-(trifluoromethylsulfonyloxy)propionateHCID 10999437—
ReactantN-(3-chloro-2-fluorophenyl)-7-methoxy-6-{[(2-methoxyethyl)amino]methyl}quinazolin-4-amineHCID 69047438—
ProductN-({4-[(3-chloro-2-fluorophenyl)amino]-7-methoxyquinazolin-6-yl}methyl)-N-(2-methoxyethyl)-L-alanineHCID 57979812—

Reaction Steps

N-(3-Chloro-2-fluorophenyl)-7-methoxy-6-{[(2-methoxyethyl)amino]methyl}quinazolin-4-amine was coupled with ethyl O-trifluoromethanesulfonyl-D-lactate and hydrolysed using analogous methods to those described for the equivalent steps in Example 46 to give N-({4-[(3-chloro-2-fluorophenyl)amino]-7-methoxyquinazolin-6-yl}methyl)-N-(2-methoxyethyl)-L-alanine; 1H NMR Spectrum: (DMSO-d6) 1.28 (d, 3H); 2.85 (t, 2H); 3.13 (s, 3H); 3.34 (m, 2H); 3.56 (q, 1H); 3.93 (m, 5H); 7.18 (s, 1H); 7.28 (t, 1H); 7.48 (t, 1H); 7.57 (m, 1H); 8.41 (m, 2H); 9.70 (brs, 1H); Mass Spectrum: (M+H)+ 463.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07632840B2
Source datasetuspto-grants-2009_12
ORD IDord-d65503f0bfa34567bf7c6a582df224c5
Source noteuspto-grants-2009_12