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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1508721Generated: October 29, 2026

Hydrochloric Acid → HCID 178477973, compound

https://huagongshe.com/reaction/1508721

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAzidotrimethylsilaneHCID 78378—
ReactantTetrabutylammonium Fluoride TrihydrateHCID 11726816—
ReactantHCID 74220974HCID 74220974—
SolventDichloromethaneHCID 6344—
ProductHCID 178477973HCID 17847797348.8%

Reaction Conditions

Temperature110 °C

Reaction Steps

In an 4-mL was charged with 2-[4-[[2-(5-Chloro-2-thienyl)-6,7-dihydro-5H-cyclopenta[d]pyrimidin-4-yl]amino]phenyl]acetonitrile (20 mg, 0.055 mmol), azidotrimethylsilane (80 mg, 1.44 mmol) and tetrabutylammonium fluoride trihydrate (25 mg, 0.07 mmol). The mixture was stirred at 110° C. overnight. After cooling to room temperature, the mixture was dissolved in dichloromethane (2 ml) and 2N HCl (aq.) (1 ml) was added. The precipitate was collected by filtration and washed with water (5 ml) followed dichloromethane (5 ml). The solid thus obtained was further triturated with dichloromethane (4 ml) to give the title compound (11 mg, 45% yield, HCl salt, it is regioisomers). MW/HCl=446.36. 1H NMR (DMSO-D6, 360 MHz) δ 7.76 (m, 3H), 7.30 (d, J=7.9 Hz, 2H), 7.23 (d, J=3.6 Hz, 1H), 4.29 (s, 2H), 2.92 (t, J=6.8 Hz, 2H), 2.86 (t, J=6.8 Hz, 2H), 2.11 (t, J=6.8 Hz, 2H). MS: ESI+, m/z 410 [M+H]+. LCMS: 97%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221843B2
Source datasetuspto-grants-2015_12
ORD IDord-dda4e7e4bb434456887e5fc15457d0c8
Source noteuspto-grants-2015_12