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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1672787Generated: October 31, 2026

Trifluoroacetic acid → HCID 86643698, compound

https://huagongshe.com/reaction/1672787

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTriethylamineHCID 8471—
ReactantHCID 67350136HCID 67350136—
SolventDichloromethaneHCID 6344—
ProductHCID 86643698HCID 8664369893.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

(S)-3-(9-Methylthio-6-oxo-2,3,3a,4-tetrahydro-1H,6H-5,8,10,10b-tetraazabenzo[e]azulen-5-yl)benzoic hydrazide (257 mg, 0.67 mmol) obtained in Step 2 of Example 56 was dissolved in dichloromethane (8.0 mL), and the mixture was cooled to 0° C. after adding triethylamine (0.19 mL, 1.34 mmol). Thereafter, anhydrous trifluoroacetic acid (0.19 mL, 1.34 mmol) was added dropwise to the mixture, and the mixture was stirred at room temperature for 30 minutes. The mixture was concentrated under reduced pressure, and a 3 mol/L aqueous sodium hydroxide solution was added to the resulting residue to adjust the pH at 4. The precipitated white solid was then filtered off to obtain (S)-3-(9-methylthio-6-oxo-2,3,3a,4-tetrahydro-1H,6H-5,8,10,10b-tetraazabenzo[e]azulen-5-yl)-N′-(2,2,2-trifluoroacetyl)benzoic hydrazide (300 mg, 93%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07998954B2
Source datasetuspto-grants-2011_08
ORD IDord-0d77ee09680d44ebb763013b6e2fe115
Source noteuspto-grants-2011_08