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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2417462Generated: November 2, 2026

Triethylamine → 2-[4-(4-chlorobenzoyl)-2-oxo-2,3,4,5-tetrahydrobenzo[e][1,4]diazepin-1-yl]-N-pyridin-3-ylacetamide Mono(trifluoroacetate)

https://huagongshe.com/reaction/2417462

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant3-AminopyridineHCID 10009—
ReactantHCID 69892979HCID 69892979—
Solvent1,1-DichloroethaneHCID 6365—
Product2-[4-(4-chlorobenzoyl)-2-oxo-2,3,4,5-tetrahydrobenzo[e][1,4]diazepin-1-yl]-N-pyridin-3-ylacetamide Mono(trifluoroacetate)HCID 22632575—

Reaction Steps

20 mg (0.042 mmol) of [4-(4-chlorobenzoyl)-2-oxo-2,3,4,5-tetrahydrobenzo[e][1,4]diazepin-1-yl]acetic acid trifluoroacetate was dissolved in 2 ml of dichloroethane. 5 mg (0.055 mmol) of 3-aminopyridine, 11 mg (0.055 mmol) of 2-chloro-1,3-dimethylimidazonium chloride and 0.018 ml (0.126 mmol) of triethylamine were added to the obtained solution, and they were stirred overnight. The solvent was evaporated, and the obtained crude product was treated in the same manner as in step 3 in Example 1 to obtain the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06825191B2
Source datasetuspto-grants-2004_11
ORD IDord-6e7fca0842f2423c8be0a061c7bd098d
Source noteuspto-grants-2004_11