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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 533764Generated: October 29, 2026

Acetic Anhydride → HCID 46843682, compound

https://huagongshe.com/reaction/533764

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantTriethylamineHCID 8471—
ReactantHCID 46843600HCID 46843600—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 46843682HCID 4684368215.6%

Reaction Steps

(3-Fluoro-4-methyl-phenyl)-(6,7,8,9-tetrahydro-5H-dipyrido[2,3-b;3′,4′-d]pyrrol-4-yl)-amine (50 mg, 0.17 mmol), acetic anhydride (17 μL, 0.17 mmol), and triethylamine (70 μL, 0.51 mmol) were dissolved in 1,2-dichloroethane (2 mL), and stirred overnight at room temperature. The reaction was quenched with H2O, and the resulting material was filtered through an Extrelut column. The Extrelut column was washed with EtOAc, and the filtrate was concentrated. The crude material was purified via Biotage eluting with a gradient of 0 to 10% MeOH in DCM. Lyophilization of the purified product provided 58 (9 mg, 14% yield) as a tan powder. LC-MS (M+H=339, obsd.=339).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08853391B2
Source datasetuspto-grants-2014_10
ORD IDord-bf11a535985a4fd681ada05ef0b8ee70
Source noteuspto-grants-2014_10