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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 507236Generated: October 30, 2026

Chloroacetyl chloride → HCID 59432898, compound

https://huagongshe.com/reaction/507236

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetyl chlorideHCID 6577—
ReactantTriethylamineHCID 8471—
ReactantHCID 43119857HCID 43119857—
SolventDichloromethaneHCID 6344—
ProductHCID 59432898HCID 5943289847.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

Under N2, a solution of 1,2,3,4-Tetrahydro-quinoline-6-sulfonic acid thiazol-2-ylamide (50 mg, 0.17 mmol), Et3N (17 mg, 24 μl, 0.17 mmol) and CH2Cl2 (0.5 mL) was cooled to 0° C. Chloroacetyl chloride (77 mg, 56 μl, 0.68 mmol) was added dropwise, over a period of 10 minutes. This reaction mixture was stirred at 0° C. for 2 hours. The mixture was purified via silica gel chromatography using 2% MeOH in CH2Cl2 to obtain the amide (30 mg, 0.08 mmol, 47% yield). LC/MS (10-99%) M/Z: M+1 obs=372.1; tR=2.51 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07786137B2
Source datasetuspto-grants-2010_08
ORD IDord-cd83100d6dff4d81a50e5f8a38642116
Source noteuspto-grants-2010_08