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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1455754Generated: October 31, 2026

Acetic Anhydride → HCID 57531447, compound

https://huagongshe.com/reaction/1455754

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 57531599HCID 57531599—
SolventChloroformHCID 6212—
ProductHCID 57531447HCID 57531447—

Reaction Steps

To a vial containing (1S)-N-{[4-(aminomethyl)-2-(2,6-diethylphenyl)-6-methylpyrimidin-5-yl]methyl}-N-methyl-1,2,3,4-tetrahydronaphthalen-1-amine (9 mg, 0.021 mmol) in CHCl3 (2.0 mL) is added acetic anhydride (0.05 mL, 25.0 eq., 0.53 mmol) and allowed to stir at room temperature for 2 h. All solvent is then removed and excess acetic anhydride is removed azeotropically with toluene (3×2 mL). The sample is re-dissolved in CHCl3 and eluted through a plug of SiO2, washing with CHCl3. Concentration affords the title compound as a colorless gum. [mass expected (470.65); mass found (470.34)].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07482350B2
Source datasetuspto-grants-2009_01
ORD IDord-db07e66829b74e9e912f73dab58a2b21
Source noteuspto-grants-2009_01