Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1444600Generated: October 31, 2026

Trifluoroacetic acid → HCID 11633317, compound

https://huagongshe.com/reaction/1444600

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTriethylamineHCID 8471—
ReactantThiophene-3-sulfonyl ChlorideHCID 2776378—
ReactantHCID 68678451HCID 68678451—
SolventDichloromethaneHCID 6344—
ProductHCID 11633317HCID 1163331766.9%

Reaction Conditions

Temperature0 °C

Reaction Steps

Trifluoroacetic acid 7.3 ml (96 mmol) was added to a solution of 2-(4-ethyl-benzoylamino)-7,8-dihydro-5H-pyrido[4,3-d]pyrimidine-6-carboxylic acid tert-butyl ester 567 mg (1.48 mmol) in CH2Cl2 (10 ml) under nitrogen as inert gas and stirring was performed for 1.5 h at RT. After removal of the solvent, the intermediate (4-ethyl-N-(5,6,7,8-tetrahydro-pyrido[4,3-d]pyrimidin-2-yl)-benzamide trifluoroacetate) was dissolved in CH2Cl2 (10 ml). After the addition of triethylamine 1150 μl (8.20 mmol), the solution was cooled to 0° C. and 3-thiophene sulfonyl chloride 253 mg (1.39 mmol) was added. The reaction mixture was stirred for 1 h at 0° C. and then overnight at RT. After removal of the solvent, purification was performed by means of column chromatography and the product 4-ethyl-N-[6-(thiophene-3-sulfonyl)-5,6,7,8-tetrahydro-pyrido[4,3-d]pyrimidin-2-yl]-benzamide 400 mg (0.93 mmol, 63% of theoretical) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07662828B2
Source datasetuspto-grants-2010_02
ORD IDord-b902e15aeb8e4ae1a0f61eb62b19a347
Source noteuspto-grants-2010_02