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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 254054Generated: November 3, 2026

Sodium borohydride → HCID 66843270, compound

https://huagongshe.com/reaction/254054

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 66842984HCID 66842984—
CatalystAcetic AcidHCID 176—
SolventMethanolHCID 887—
ProductHCID 66843270HCID 6684327083.3%

Reaction Steps

(2R)-3-(4-cyanophenyl)-2-{[({[4-((2R,3R)-1-(4-fluorophenyl)-3-{[2-(4-fluorophenyl)-2-oxoethyl]thio}-4-oxoazetidin-2-yl)phenoxy]acetyl}amino}acetyl]amino)propanoic acid (0.006 g, 0.0084 mmole) was dissolved in methanol (1.5 ml). NaBH4 (0.0035 g, 0.092 mmole) was added and when the reaction was complete according to LC-MS a few drops of acetic acid was added. The solvent was removed under reduced pressure and the residue was purified by preparative HPLC on a Kromasil C8-column using a stepwise gradient of 33.5%, 43% and then 55.5% MeCN in 0.1M ammonium acetate buffer as eluent. After freeze-drying, 0.005 g (83%) of the desired product was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07871998B2
Source datasetuspto-grants-2011_01
ORD IDord-c3019296f6b749bf97ee1272159a5c63
Source noteuspto-grants-2011_01