HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 382649Generated: October 29, 2026
Iodomethyl pivalate → HCID 131722928, compound
https://huagongshe.com/reaction/382649
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodomethyl pivalate | HCID 104401 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 131722929 | HCID 131722929 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 131722928 | HCID 131722928 | — |
Reaction Steps
To a solution of 40 mg of sodium (1S,5R,6S)-6-((1R)-1-hydroxyethyl)-2-(7-methoxymethylimidazo[5,1-b]thiazol-2-yl)-1-methyl-1-carbapen-2-em-3-carboxylate in 0.6 ml of DMF was added 4.2 mg of sodium hydrogen carbonate, and the mixture was cooled to −30° C. under the atmosphere of argon. Pivaloyloxymethyl iodide (34 mg) was added, and the mixture was stirred for 1 hour, diluted with 30 ml of ethyl acetate, and washed with 20 ml of saturated aqueous saline and 20 ml of semi-saturated squeous saline. The organic layer was dried over anhydrous magnesium sulfate, and concentrated under reduced pressure to a volume of about 1 ml. The concentrate was purified by column chromatography on silica gel (chloroform:methanol=95:5) to give the title compound was obtained in a yield of 18.4 mg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06310056B1 |
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| Source dataset | uspto-grants-2001_10 |
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| ORD ID | ord-c1c7cffbae5e415697d77e017ed7cb75 |
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| Source note | uspto-grants-2001_10 |
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