HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 568254Generated: October 31, 2026
1-Acetoxy-2-bromoethane → HCID 178459454, compound
https://huagongshe.com/reaction/568254
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Acetoxy-2-bromoethane | HCID 13564 | — |
| Reactant | Allyl(1R,5S,6S)-2-[(3S,5S)-1-allyloxycarbonyl-5-(5-methylimidazo[5,1-b]thiazol-2-yl)methylpyrrolidin-3-yl]thio-6-((1R)-1-hydroxyethyl)-1-methylcarbapen-2-em-3-carboxylate | HCID 131722343 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 178459454 | HCID 178459454 | — |
Reaction Steps
Bromoethyl acetate (0.04 ml) is added to a solution of 42.6 mg of allyl(1R,5S,6S)-2-[(3S,5S)-1-allyloxycarbonyl-5-(5-methylimidazo[5,1-b]thiazol-2-yl)methylpyrrolidin-3-yl]thio-6-((1R)-1-hydroxyethyl)-1-methylcarbapen-2-em-3-carboxylate, described in Example 31-a), in 0.7 ml of dry acetone, and the mixture is stirred in an argon atmosphere at room temperature for one hr. The solvent is removed by evaporation under reduced pressure. The residue is purified by column chromatography on Sephadex LH-20 (dichloromethane:methanol=1:1) to give 49.7 mg of allyl(1R,5S,6S)-2-[(3S,5S)-1-allyloxycarbonyl-5-[6-ethoxycarbonylmethyl-5-methylimidazo[5,1-b]thiazolium-2-yl]methylpyrrolidin-3-yl]thio-6-((1R)-1-hydroxyethyl)-1-methylcarbapen-2-em-3-carboxylate bromide as a brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06180622B2 |
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| Source dataset | uspto-grants-2001_01 |
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| ORD ID | ord-f3c9554fe6aa4d7a85539bb506c58c23 |
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| Source note | uspto-grants-2001_01 |
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