Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 518728Generated: October 31, 2026

Thionyl Chloride → HCID 178522615, compound

https://huagongshe.com/reaction/518728

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 178522616HCID 178522616—
SolventDichloromethaneHCID 6344—
ProductHCID 178522615HCID 17852261596.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a 0° C. suspension of cis-4-((E)-2-(4-fluorobenzoylimino)-6-(morpholinomethyl)-2,3-dihydro-1H-benzo[d]imidazol-1-yl)cyclohexanecarboxylic acid (0.5 g, 1.041 mmol) in DCM (10.41 mL) was added thionyl chloride (0.380 mL, 5.20 mmol). The suspension was stirred for 30 minutes at 0° C. The reaction was concentrated, resuspended in ACN (5 mL), and reconcentrated to generate cis-4-((E)-2-(4-fluorobenzoylimino)-6-(morpholinomethyl)-2,3-dihydro-1H-benzo[d]imidazol-1-yl)cyclohexanecarbonyl chloride (0.50 g, 96% yield) as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115127B2
Source datasetuspto-grants-2015_08
ORD IDord-c65c6a5dcc3d4dc48a1833ba30bc724a
Source noteuspto-grants-2015_08