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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 497396Generated: October 29, 2026

Water → 3,4,5,6-Tetrahydro-3,8,10-triaza-benzo[e]azulene-1-carboxylic acid 2-fluoro-phenyl-amide

https://huagongshe.com/reaction/497396

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant2-FluoroanilineHCID 9584—
ReactantTrimethylaluminumHCID 16682925—
Reactant3,4,5,6-Tetrahydro-3,8,10-triaza-benzo[e]azulene-1-carboxylic acid ethyl esterHCID 20605615—
SolventDichloromethaneHCID 6344—
SolventAmmonium ChlorideHCID 25517—
Product3,4,5,6-Tetrahydro-3,8,10-triaza-benzo[e]azulene-1-carboxylic acid 2-fluoro-phenyl-amideHCID 2060559372%

Reaction Steps

To a solution of 2-fluoroaniline (108 mg, 0.972 mmol) in CH2Cl2 (2.0 mL) at 0° C. under N2 is slowly added AlMe3 (0.49 mL, 2.0 M in toluene). The resulting solution is stirred at room temperature for 1 h. Next, 3,4,5,6-tetrahydro-3,8,10-triaza-benzo[e]azulene-1-carboxylic acid ethyl ester (50 mg, 0.194 mmol) is added in one portion. The resulting mixture is then stirred at reflux for 2 h. After cooling, the reaction mixture is carefully diluted with saturated aq NH4Cl (˜5 mL) and some H2O. The mixture is stirred vigorously for 15 min. and then extracted three times with CH2Cl2. The combined extracts are dried over K2CO3 and concentrated. The crude material is purified by flash chromatography on silica gel. Elution with 40:1 CHCl3—MeOH followed by 30:1 CHCl3—MeOH and finally 20:1 CHCl3—MeOH afforded 45 mg (72%) of 3,4,5,6-tetrahydro-3,8,10-triaza-benzo[e]azulene-1-carboxylic acid (2-fluoro-phenyl)-amide as a light yellow solid. Electrospray mass spectrum: m/z 321 [M−1].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06949562B2
Source datasetuspto-grants-2005_09
ORD IDord-5e94b577676e4826b529eecf3e2836be
Source noteuspto-grants-2005_09