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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 578627Generated: November 1, 2026

Sodium Hydroxide → 4-{[3-(Trifluoromethyl)benzyl]amino}quinazoline-8-carboxylic acid

https://huagongshe.com/reaction/578627

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantMethyl 4-{[3-(trifluoromethyl)benzyl]amino}quinazoline-8-carboxylateHCID 66763817—
SolventMethanolHCID 887—
Product4-{[3-(Trifluoromethyl)benzyl]amino}quinazoline-8-carboxylic acidHCID 6676378389%

Reaction Steps

A solution of methyl 4-{[3-(trifluoromethyl)benzyl]amino}quinazoline-8-carboxylate (95 mg, 0.26 mmol) in 5 mL of MeOH was treated with 2N NaOH (650 μL, 1.3 mmol, 5 equiv.) under refluxing for 5 h. After removal of MeOH, water was added to the residue and pH was adjusted to ˜4 with 2N HCl. The precipitate was collected as the desired acid by filtration, and washing with water in 89% yield. 1HNMR (in DMSO): 4.96 (d, J=5.8 Hz, 2H), 7.56-7.61 (m, 1H), 7.64 (d, J=7.7 Hz, 1H), 7.70 (d, J=7.7 Hz, 1H), 7.74-7.78 (m, 2H), 8.54 (dd, J=1.2 and 7.4 Hz, 1H), 8.63 (dd, J=1.2 and 7.3 Hz, 1H), 8.69 (s, 1H), 9.68 (d, J=5.8 Hz, 1H). Mass: M+H+: 348.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09040560B2
Source datasetuspto-grants-2015_05
ORD IDord-e9bd6d219a9b480c8085d1052327eb7c
Source noteuspto-grants-2015_05