HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1370621Generated: October 28, 2026
Bromomethyl acetate → HCID 69942568, compound
https://huagongshe.com/reaction/1370621
Participants
| Role | Name | HCID | Charge |
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| Reactant | Bromomethyl acetate | HCID 68536 | — |
| Reactant | HCID 3002971 | HCID 3002971 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 69942568 | HCID 69942568 | — |
Reaction Steps
To a mixture of 1-[(1R,2R)-2-(2,4-difluorophenyl)-2-hydroxy-1-methyl-3-(1H-1,2,4-triazol-1-yl)propyl]-3-[4-(1H-1,2,3-triazol-1-yl)phenyl]-2-imidazolidinone (0.5 g) and acetonitrile (10 ml) was added bromomethyl acetate (0.1 ml), and the mixture was stirred for 24 hours at 50° C. The reaction mixture was purified by silica gel flush chromatography (silica gel 25 g, eluent: ethyl acetate→acetone→acetone/ethanol=10/1). The residue purified was crystallized from ethanol to give 4-acetoxymethyl-1-[(2R,3R)-2-(2,4-difluorophenyl)-2-hydroxy-3-[2-oxo-3-[4-(1H-1,2,3-triazol-1-yl)phenyl]-1-imidazolidinyl]butyl]-1H-1,2,4-triazolium bromide (Compound 10, 0.135 g) as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06583164B1 |
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| Source dataset | uspto-grants-2003_06 |
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| ORD ID | ord-17e6feea34914d519e5ca3a168c8441a |
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| Source note | uspto-grants-2003_06 |
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