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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2182370Generated: November 1, 2026

Chloroacetyl chloride → HCID 178422294, compound

https://huagongshe.com/reaction/2182370

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetyl chlorideHCID 6577—
ReactantMorpholineHCID 8083—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 178422296HCID 178422296—
SolventDichloromethaneHCID 6344—
ProductHCID 178422294HCID 178422294—

Reaction Steps

A stirred solution of 3-(5,6-dimethyl-1H-benzoimidazol-2-yl)-1H-pyrazol-4-ylamine [100 mg, Example 233(c)] and diisopropylethylamine (307 μl) in dichloromethane (10 ml) was treated with chloroacetyl chloride (105 μl). The reaction mixture was stirred for 30 minutes at room temperature, then treated with morpholine (575 μl), then kept at room temperature overnight and then evaporated. The oily residue was partitioned between ethyl acetate and water and the organic phase was washed with water, then dried over magnesium sulfate and then evaporated. The residue was subjected to flash chromatography on silica eluting with ethyl acetate to give the N-[3-(5,6-dimethyl-1H-benzoimidazol-2-yl)-1H-pyrazol-4-yl]-2-morpholin-4-yl-acetamide (49.9 mg) as an off-white solid. MS: 355.68 (M+H)+. HPLC (METHOD B1): RT=8.28 minutes. (b) 2-Dimethylamino-N-[3-(5,6-dimethyl-1H-benzoimidazol-2-yl)-1H-pyrazol-4-yl]-acetamide

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06897208B2
Source datasetuspto-grants-2005_05
ORD IDord-fa9312ce9c7c4992b396d4fc22756ded
Source noteuspto-grants-2005_05