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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 540861Generated: October 26, 2026

Acetyl chloride → N-[1,1-dimethyl-2-(3-nitro-7-benzyloxyquinolin-4-ylamino)ethyl]acetamide

https://huagongshe.com/reaction/540861

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantTriethylamineHCID 8471—
Reactant(2-Amino-2-methylpropyl)(7-benzyloxy-3-nitroquinolin-4-yl)amineHCID 67050934—
SolventDichloromethaneHCID 6344—
ProductN-[1,1-dimethyl-2-(3-nitro-7-benzyloxyquinolin-4-ylamino)ethyl]acetamideHCID 68897784—

Reaction Conditions

Temperature0 °C

Reaction Steps

Under a nitrogen atmosphere, a solution of (2-amino-2-methylpropyl)(7-benzyloxy-3-nitroquinolin-4-yl)amine (6.5 g, 17.5 mmol), prepared in Part A of Example 45, in dichloromethane (200 mL) was cooled to 0° C.; triethylamine (4.87 mL, 35.0 mmol) and acetyl chloride (1.37 mL, 19.2 mmol) were sequentially added. The reaction was stirred at 0° C. for 30 minutes, allowed to warm to ambient temperature, and stirred for three hours. The reaction was washed with saturated aqueous sodium bicarbonate (2×) and brine, dried over sodium sulfate, filtered, and concentrated under reduced pressure to provide N-[1,1-dimethyl-2-(3-nitro-7-benzyloxyquinolin-4-ylamino)ethyl]acetamide as a yellow powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871782B2
Source datasetuspto-grants-2014_10
ORD IDord-31b1627072e3418a98af563f0a868a2a
Source noteuspto-grants-2014_10