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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 339768Generated: October 29, 2026

Trifluoroacetic acid → HCID 178493831, compound

https://huagongshe.com/reaction/339768

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 178493819HCID 178493819—
SolventMethanolHCID 887—
ProductHCID 178493831HCID 178493831113.7%

Reaction Conditions

Temperature60 °C

Reaction Steps

N-[8-(Benzyloxy)-7-methoxy-2,3-dihydroimidazo[1,2-c]quinazolin-5-yl]nicotinamide (20 g, 45.1 mmol) was added portionwise over 1 h to a round bottom flask containing TFA (400 mL) precooled with an ice bath. The reaction mixture was heated to 60° C. and allowed to stir at this temperature for 17 h at which time it was cooled to room temperature. The reaction mixture was then concentrated under reduced pressure. The resulting residue was dissolved in CH2Cl2 and hexane and concentrated under reduced pressure. The material thus obtained was dissolved in MeOH and CH2Cl2 (250 mL, 1:1) and concentrated under reduced pressure. The resulting solids were dried overnight under vacuum with low heat to give N-(8-hydroxy-7-methoxy-2,3-dihydroimidazo[1,2-c]quinazolin-5-yl)nicotinamide (17.3 g, 66%): 1H NMR (DMSO-d6+2 drops TFA-d) δ: 13.41 (1H, s), 12.21 (1H, br s), 9.38 (1H, s), 8.78 (1H, d), 8.53 (1H, d), 7.85 (1H, d), 7.59 (1H, m), 7.17 (1H, d), 4.54 (2H, m), 4.21 (2H, m), 3.98 (3H, s); mass spectrum m/z 481 ((M+1)+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08895549B2
Source datasetuspto-grants-2014_11
ORD IDord-09157085d659441296afeb5ec675274a
Source noteuspto-grants-2014_11