HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 727617Generated: November 1, 2026
Diphenylphosphinic chloride → HCID 131720430, compound
https://huagongshe.com/reaction/727617
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diphenylphosphinic chloride | HCID 73910 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1-Azabicyclo[3.2.0]heptane-2-carboxylic acid, 6-[(1R)-1-hydroxyethyl]-4-methyl-3,7-dioxo-, (4-nitrophenyl)methyl ester, (4R,5R,6S)- | HCID 9885302 | — |
| Reactant | HCID 88299975 | HCID 88299975 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 131720430 | HCID 131720430 | 39.2% |
Reaction Steps
7.0 g of diphenylphosphoryl chloride and 3.4 g of diisopropylethylamine were added dropwise, whilst ice-cooling, to a solution of 8.6 g of 4-nitrobenzyl (1R,5R,6S)-6-[(1R)-1-hydroxyethyl]-1-methyl-2-oxo-1-carbapenam-3-carboxylate in 120 ml of dry acetonitrile, and the resulting mixture was stirred at the same temperature for 1 hour. 6.7 g of diisopropylethylamine and a solution of 13.8 g of (2S,4S)-4-mercapto-2-[4-(4-nitrobenzyloxycarbonyl)-1-piperazinylcarbonyl]-1-methylpyrrolidine trifluoromethanesulfonate in dry acetonitrile were then simultaneously added dropwise to the mixture, whilst ice-cooling, and the resulting mixture was allowed to stand overnight, whilst ice-cooling. At the end of this time, the reaction mixture was worked up and purified in a similar manner to that described in Example 49(a), to give 7.0 g of the title compound, as a powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05712267 |
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| Source dataset | uspto-grants-1998_01 |
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| ORD ID | ord-645d79e9d1454b16945f839ad6656b72 |
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| Source note | uspto-grants-1998_01 |
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