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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1911286Generated: October 31, 2026

Acetic Anhydride → N-(Isoquinolin-3-yl)acetamide

https://huagongshe.com/reaction/1911286

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantTriethylamineHCID 8471—
ReactantIsoquinolin-3-AmineHCID 311869—
SolventDichloromethaneHCID 6344—
ProductN-(Isoquinolin-3-yl)acetamideHCID 12366594100%

Reaction Steps

Acetic anhydride (5.92 mL, 62.6 mmol) was added to a suspension of isoquinolin-3-amine (3.01 g, 20.9 mmol) and triethylamine (3.18 mL, 23.0 mmol) in CH2Cl2 (80 mL) at ambient temperature. The mixture was stirred 3.5 hours, then the volatiles were evaporated in vacuo. The residue was chased with toluene and concentrated in vacuo (3×25 mL) to provide the title compound (3.89 g) as a yellow solid. This material, which was found to also contain small quantities of acetic acid, was used without further purification. 1H NMR (300 MHz, DMSO-d6) δ 10.58 (s, 1H), 9.13 (s, 1H), 8.45 (s, 1H), 8.04 (d, J=7.8 Hz, 1H), 7.88 (d, J=8.2 Hz, 1H), 7.69 (ddd, J=8.2, 6.8, 1.2 Hz, 1H), 7.52 (ddd, J=7.9, 6.9, 1.0 Hz, 1H), 2.13 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08604053B2
Source datasetuspto-grants-2013_12
ORD IDord-5c22ace4cba84948a65cbe9b26b70228
Source noteuspto-grants-2013_12