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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1914554Generated: October 30, 2026

Dichloromethane → Azepan-1-yl-(5-pyridin-4-yl-thiophen-3-yl)-methanone

https://huagongshe.com/reaction/1914554

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantN-AcetylhomopiperazineHCID 4186202—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Reactant5-Pyridin-4-yl-thiophene-3-carboxylic acidHCID 58110228—
SolventAcetonitrileHCID 6342—
ProductAzepan-1-yl-(5-pyridin-4-yl-thiophen-3-yl)-methanoneHCID 4422446228.8%

Reaction Steps

5-Pyridin-4-yl-thiophene-3-carboxylic acid (0.4 mmol) was dissolved in MeCN (2 mL). 1-[1,4]Diazepan-1-yl-ethanone (1.8 mmol), and HATU (0.4 mmol) were added and the reaction mixture stirred for 72 hours. DCM (20 mL) was added and the organic solution was separated and the solvent removed by evaporation. The residue was purified by HPLC, eluting with 10%-90% acetonitrile in water (0.1% formic acid) over 30 minutes. The fractions containing the desired product were concentrated under vacuum and freeze-dried to give the title compound as a white solid (33 mg). LCMS m/z 287.09 [M+H]+ RT=5.20 min. (Analytical Method 2). 1H NMR (400 MHz, MeCN-d): δ 8.6 (d, 2H), 7.95 (d, 2H), 7.9 (s, 1H), 7.8 (s, 1H), 3.6 (t, 2H), 3.5 (t, 2H), 1.8-1.6 (m, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08614209B2
Source datasetuspto-grants-2013_12
ORD IDord-72e456684d454ab8ab41a2981dbf7f33
Source noteuspto-grants-2013_12