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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1396621Generated: October 31, 2026

Triethylamine → (S)-N-(1-(8-chloro-1-(2-morpholinoethyl)isoquinolin-3-yl)ethyl)thiazolo[5,4-d]pyrimidin-7-amine

https://huagongshe.com/reaction/1396621

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant7-Chlorothiazolo[5,4-D]pyrimidineHCID 263007—
Reactant(S)-1-(8-chloro-1-(2-morpholinoethyl)isoquinolin-3-yl)ethanamineHCID 68747373—
Solvent1-ButanolHCID 263—
Product(S)-N-(1-(8-chloro-1-(2-morpholinoethyl)isoquinolin-3-yl)ethyl)thiazolo[5,4-d]pyrimidin-7-amineHCID 57330000—

Reaction Steps

A mixture of (S)-1-(8-chloro-1-(2-morpholinoethyl)isoquinolin-3-yl)ethanamine 71 (100 mg, 0.31 mmol, 1 eq), 7-chlorothiazolo[5,4-d]pyrimidine (E-4) (108 mg, 0.63 mmol, 2 eq) and triethylamine (130 mg, 1.25 mmol, 4.0 eq) in n-BuOH (40 mL) was stirred at reflux for 16 h. The reaction mixture was cooled to RT and concentrated in vacuo. The residue was purified by flash column chromatography on silica gel (1-5% MeOH-DCM) to afford the product (S)—N-(1-(8-chloro-1-(2-morpholinoethyl)isoquinolin-3-yl)ethyl)thiazolo[5,4-d]pyrimidin-7-amine 72. ESI-MS m/z: 455.0 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901133B2
Source datasetuspto-grants-2014_12
ORD IDord-90b4a6da34e944ff9f175dbadc674060
Source noteuspto-grants-2014_12