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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1161271Generated: October 29, 2026

Methanol → HCID 59411473, compound

https://huagongshe.com/reaction/1161271

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantTriethylamineHCID 8471—
Reactant2-Amino-2-methyl-1-propanolHCID 11807—
Reactant5-nitro-1H-isochromen-1-oneHCID 10012760—
ProductHCID 59411473HCID 59411473—

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 5-nitro-isochromen-1-one (1.02 g, 0.00480 mol), 2-amino-2-methyl-1-propanol (0.921 mL, 0.00960 mol) and methanol (23 mL, 0.58 mol) and triethylamine (2 mL, 0.01 mol) was stirred overnight at 80° C. LC-MS analysis showed the formation of the desired product. Volatiles were removed under reduced pressure and the residue was taken up in a mixture of methylene chloride (20 mL, 0.3 mol) and N,N-dimethylformamide (0.85 mL, 0.011 mol). Acetyl chloride (1.0 mL, 0.014 mol) and N,N-diisopropylethylamine (1.5 mL, 0.0088 mol) were added. The mixture was allowed to stir at 40° C. for 5 hours. The flask was cooled to room temperature and solvents were removed in vacuo. The residue was taken up in Ethyl acetate and washed twice with aqueous NaHCO3. The organic layer was dried with Sodium sulfate and concentrated under reduced pressure. The residue was purified by column chromatography using an Ethyl acetate: Hexane (0-100%) gradient to obtain the desired product. M+1=263.2

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07816371B2
Source datasetuspto-grants-2010_10
ORD IDord-b4764536f13f4762852a5c902091b4e0
Source noteuspto-grants-2010_10