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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1364061Generated: October 29, 2026

Chloroacetyl chloride → HCID 66958446, compound

https://huagongshe.com/reaction/1364061

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetyl chlorideHCID 6577—
ReactantTriethylamineHCID 8471—
ReactantTert-butyl 2-[(3-amino-7-benzyloxyquinolin-4-yl)amino]ethylcarbamateHCID 66958391—
SolventDichloromethaneHCID 6344—
ProductHCID 66958446HCID 6695844615.5%

Reaction Steps

Triethylamine (24.0 mL, 172.58 mmol) was added to a solution of tert-butyl 2-[(3-amino-7-benzyloxyquinolin-4-yl)amino]ethylcarbamate (35.25 g, 86.29 mmol) in dichloromethane (400 mL), and the reaction was stirred at ambient temperature. Chloroacetyl chloride (6.87 mL, 86.29 mmol) was quickly added at ambient temperature, and the reaction was stirred for 10 minutes. The reaction mixture was concentrated under reduced pressure, and the residue was dissolved in ethanol (500 mL) and stirred for two days at ambient temperature. The mixture was concentrated under reduced pressure and the residue was recrystallized from dichloromethane to afford 6.23 g of tert-butyl 2-[7-benzyloxy-2-(chloromethyl)-1H-imidazo[4,5-c]quinolin-1-yl]ethylcarbamate. The mother liquor was divided into two portions which were separately purified by normal phase prep HPLC on silica gel (eluting with 2 N ammonia in methanol/chloroform in a 33-minute gradient from 0:100 to 5:95) and combined to provide an additional 24.21 g of product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07888349B2
Source datasetuspto-grants-2011_02
ORD IDord-0404af802274443c97aee294602fcbb5
Source noteuspto-grants-2011_02