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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 533763Generated: October 30, 2026

Acetic Anhydride → HCID 46843681, compound

https://huagongshe.com/reaction/533763

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantTriethylamineHCID 8471—
ReactantHCID 66677449HCID 66677449—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 46843681HCID 4684368122%

Reaction Steps

Naphthalen-1-yl-(6,7,8,9-tetrahydro-5H-dipyrido[2,3-b;3′,4′-d]pyrrol-4-yl)-amine (40 mg, 0.13 mmol), acetic anhydride (12 μL, 0.13 mmol), and triethylamine (53 μL, 0.38 mmol) were dissolved in 1,2-dichloroethane (2 mL), and stirred for 3 h at room temperature. The reaction mixture was added directly to a Biotage column. The crude product was purified via Biotage eluting with a gradient of 0 to 10% MeOH in DCM. Lyophilization of the purified product provided 57 (10 mg, 22% yield) as a tan powder. LC-MS (M+H=357, obsd.=357).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08853391B2
Source datasetuspto-grants-2014_10
ORD IDord-23317b123af047d498f77b75f9d0e489
Source noteuspto-grants-2014_10