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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2223134Generated: October 31, 2026

Acetic Acid → HCID 21072800, compound

https://huagongshe.com/reaction/2223134

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 21072805HCID 21072805—
ReactantHCID 21072852HCID 21072852—
SolventEthanolHCID 702—
ProductHCID 21072800HCID 21072800—

Reaction Conditions

Temperature50 °C

Reaction Steps

900 mg (2.5 mmol) of 5-benzyloxy-8-(2-ethoxy-2-hydroxyacetyl)-4H-benzo[1,4]oxazin-3-one and 700 mg (2.7 mmol) of 1-[2-(1-aminocyclopropyl)ethyl]-4,4-dimethyl-1,4-dihydrobenzo [d][1,3]oxazin-2-one is dissolved in 20 mL of ethanol and stirred in each case for 30 minutes at 80° C. and 50° C. The reaction mixture is cooled, combined with 200 mg (5.3 mmol) sodium borohydride, and stirred for 2 hours at ambient temperature. Glacial acetic acid is added, the mixture is stirred for 10 minutes, and evaporated down. The residue is taken up in dichloromethane and washed successively with potassium hydrogen sulfate solution, 15% potassium carbonate solution, and sodium hydrogen carbonate solution. Then the organic phase is dried with sodium sulfate and freed from solvent. The residue is purified by column chromatography (silica gel; ethyl acetate/methanol/ammonia gradient). Recrystallization from diisopropylether. White solid. Yield: 690 mg (49%); mass spectroscopy: [M+H]+=558.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07375104B2
Source datasetuspto-grants-2008_05
ORD IDord-7e76e4c7ff904f11a6e06f3fbf46191d
Source noteuspto-grants-2008_05