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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 651689Generated: October 30, 2026

Water → Thieno[3,2-b]pyridine-2-sulfonic acid[1-(1-aminoisoquinolin-7-ylmethyl)-2-oxopyrrolidin-3-(r)-yl]amide trifluoroacetate

https://huagongshe.com/reaction/651689

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDiisopropylethylamineHCID 81531—
ReactantThieno[3,2-b]pyridine-2-sulfonyl chlorideHCID 18176395—
Reactant3-(R)-Amino-1-(1-aminoisoquinolin-7-ylmethyl)pyrrolidin-2-one trifluoroacetateHCID 20680693—
SolventAcetonitrileHCID 6342—
ProductThieno[3,2-b]pyridine-2-sulfonic acid[1-(1-aminoisoquinolin-7-ylmethyl)-2-oxopyrrolidin-3-(r)-yl]amide trifluoroacetateHCID 70122297—

Reaction Steps

3-(R)-Amino-1-(1-aminoisoquinolin-7-ylmethyl)pyrrolidin-2-one trifluoroacetate (80 mg, 0.216 mmol) and diisopropylethylamine (140 mg, 1.08 mmol) are dissolved in acetonitrile (12 mL), and stirred at room temperature for 15 minutes before adding thieno[3,2-b]pyridine-2-sulfonyl chloride dropwise as a solution in acetonitrile (8 mL). The reaction mixture is left at room temperature overnight, water (4 mL) added, and the solution concentrated in vacuo to remove the acetonitrile (ca. 4 mL of solution). 75% Acetonitrile/water (4 mL) is added. and the product purified by reverse phase preparative HPLC with gradient elution 10-40% acetonitrile/water (0.1% trifluoroacetic acid). The product fractions are combined, the acetonitrile removed in vacuo, and the aqueous solution lyophilized to give the product as a white powder (52 mg, 0.092 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06281227B1
Source datasetuspto-grants-2001_08
ORD IDord-1243990493874caea15c1fba693adeab
Source noteuspto-grants-2001_08