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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2199026Generated: October 29, 2026

Sodium Bicarbonate → HCID 131712876, compound

https://huagongshe.com/reaction/2199026

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 131712878HCID 131712878—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 131712876HCID 131712876—

Reaction Steps

A solution of p-nitrobenzyl 2-benzyloxycarbonylmethylthio-6-(1-acetoxy)ethyl-carbapen-2-em-3-carboxylate (5.6 mg, 0.01 mmol) in dioxane (0.60 ml) is diluted with ethanol (0.05 ml) and water (0.35 ml) containing sodium bicarbonate (1.0 mg, 0.012 mmol). The solution is treated with 10% palladium on charcoal (5.5 mg) and hydrogenated at 40 psi for 30 minutes. The mixture is diluted with water (3 ml) and centrifuged to remove the catalyst which is washed with more water (2×1 ml). The combined aqueous supernatant is washed with ethyl acetate (4×2 ml), filtered through a cotton plug, concentrated in vacuo to ca. 1 ml, and lyophilized to yield the title compound as an amorphous solid: UV (0.1 M pH 7 phosphate buffer) 299 nm; NMR (D2O) δ1.30 (d, 3, J=6.7, CH3), 2.13 (s, 3, COCH3), 2.81 (dd, 1, J=9 and 18, H1a), 3.05 (dd, 1, J=10 and 18, H1b), 3.31 (dd, 1, J=3 and 5, H6), ~3.7(m, SCH2, obscured by impurities), 4.07 (m, 1, H5), 5.21 (m, 1, CHCH3), 5.27(s, 2, CH2 φ) and 7.48 (s, 5, C6H5); electrophoresis in 0.05 M pH 6.9 buffer at 2 KV for 20 minutes gives a single bioactive zone moving 3-5 cm toward the anode; HPLC on a C18Bondapak Reverse phase column using 10% THF/H2O at 1.0 ml/min gives a UV visible peak at retention time 17.4 mins (4.8 mins for thienamycin).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04361512
Source datasetuspto-grants-1982_11
ORD IDord-517b7da462fa438686a8f2bcc69d4287
Source noteuspto-grants-1982_11