Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1897604Generated: October 30, 2026

Dichloromethane → HCID 69937824, compound

https://huagongshe.com/reaction/1897604

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantSodium CarbonateHCID 10340—
Reactant2-Chloro-4-(tetramethyl-1,3,2-dioxaborolan-2-yl)benzonitrileHCID 57926113—
ReactantHCID 67155049HCID 67155049—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventDimethylformamideHCID 6228—
ProductHCID 69937824HCID 699378246.1%

Reaction Conditions

Temperature100 °C

Reaction Steps

To the solution of 2-chloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzonitrile (409 mg, 1.55 mmol), 3-(3-Bromo-5-fluoro-pyridin-4-yl)-oxetan-3-ol (350 mg, 1.41 mmol) and PdCl2(dppf).CH2Cl2 adduct (115 mg, 0.141 mmol) in DMF (7 mL) was added a solution of Na2CO3 (2M in water, 1.76 ml, 3.53 mmol) under Nitrogen atmosphere. The mixture was stirred and heated at 100° C. for 4 hrs. After letting cool to room temperature, solvent was removed in vacuo. The resulting residue was dissolved in DCM and saturated NH4Cl solution. After extraction with DCM and separation, the combined extracts were concentrated and purified by ISCO 12 g (0-40%, v/v, EtOAc/Heptane) to give 2-Chloro-4-[5-fluoro-4-(3-hydroxy-oxetan-3-yl)-pyridin-3-yl]-benzonitrile (26 mg, 6%) as colorless solid; ESI-MS m/z: 305 [M++1]+, Retention time 1.27 min; 1H-NMR (CDCl3, 400 MHz) δ 4.42 (d, J=8.4 Hz, 2H), 4.66 (d, J=8.4 Hz, 2H), 7.57 (d, J=6.8 Hz, 1H), 7.76 (s, 1H), 7.80 (d, J=6.8 Hz, 1H), 8.41 (s, 1H), 8.59 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08519134B2
Source datasetuspto-grants-2013_08
ORD IDord-830cffc46ea54f5c9b21056d8d10c40d
Source noteuspto-grants-2013_08