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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 708461Generated: October 29, 2026

Sodium borohydride → HCID 118379551, compound

https://huagongshe.com/reaction/708461

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 118379844HCID 118379844—
SolventEthanolHCID 702—
ProductHCID 118379551HCID 118379551—

Reaction Steps

To a solution of tert-butyl 3-(((2R,3S)-3-(((benzyloxy)carbonyl)amino)-4-oxoazetidin-2-yl)methyl)-2,4-dioxoimidazolidine-1-carboxylate (170 mg, 0.390 mmol) in EtOH (10 mL) at 0° C. was added sodium borohydride (30 mg, 0.78 mmol). After 3 h at 0° C., the mixture was quenched with saturated NH4Cl (aq) and partially concentrated in vacuo. The bilayer was extracted with DCM and the organic layer was dried over Na2SO4 and concentrated in vacuo. The resulting residue was used as such in step 5. LCMS: m/z=457.1 (M+Na).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09174978B2
Source datasetuspto-grants-2015_11
ORD IDord-2854aa94bb9f4354823255bd0b09749d
Source noteuspto-grants-2015_11