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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 51148Generated: October 25, 2026

2-(Methylsulfonyl)ethanamine → N-(4-(3-(trifluoromethyl)benzyloxy)phenyl)-6-(5-((2-(methylsulfonyl)ethylamino)methyl)furan-2-yl)quinazolin-4-amine

https://huagongshe.com/reaction/51148

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Methylsulfonyl)ethanamineHCID 4340561—
Reactant5-(4-{4-(3-Trifluoromethylbenzyloxy)anilino}-6-quinazolinyl)-furan-2-carbaldehydeHCID 21952269—
ProductN-(4-(3-(trifluoromethyl)benzyloxy)phenyl)-6-(5-((2-(methylsulfonyl)ethylamino)methyl)furan-2-yl)quinazolin-4-amineHCID 9808725—

Reaction Steps

Prepared according to Procedure D from 5-(4-{4-(3-trifluoromethylbenzyloxy)anilino}-6-quinazolinyl)-furan-2-carbaldehyde (0.6 equiv) and 2-methanesulphonyl-ethylamine (1 equiv). 1H NMR 300 MHz (DMSO-d6) 11.63 (bs, 1H); 9.88 (bs, 1H); 9.59 (bs, 1H); 8.88 (s, 1H); 8.43 (d, 1H); 7.97 (d, 1H); 7.90-7.67 (m, 6H); 7.34 (d, 1H); 7.19 (d, 2H); 6.89 (d, 1H); 5.30 (s, 2H); 4.45 (s, 2H); 3. 78 (m, 2H); 3.45 (m, 2H, obscured by water peak); 3.19 (s, 3H); MS m/z 597 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06713485B2
Source datasetuspto-grants-2004_03
ORD IDord-d2bfad2d906b4fe9af09cb34efef75cf
Source noteuspto-grants-2004_03