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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2306204Generated: November 3, 2026

HCID 88191236, compound → HCID 70172656, compound

https://huagongshe.com/reaction/2306204

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 88191236HCID 88191236—
CatalystNickelHCID 935—
SolventEthanolHCID 702—
ProductHCID 70172656HCID 70172656—

Reaction Steps

(R)-3-(tert-Butoxycarbonylamino)-1-[7-(tert-butyldimethylsilyloxy) naphthalen-1-yl]-2-thioxopyrrolidine, as described above in Step G, (1.04 g, 2.19 mmol) was dissolved in EtOH (100 mL) and Raney Ni (5 g of a slurry in EtOH) was added. The mixture was stirred at ambient temperature for 18 hours, then an additional portion of Raney Ni (3 g of a slurry in EtOH) was added. After a further 4 hours stirring, the reaction mixture was filtered through a pad of celite, washing with EtOH. The filtrate was concentrated in vacuo to provide the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06441017B1
Source datasetuspto-grants-2002_08
ORD IDord-edf6ddce9ede4b1097775ee3aca0f889
Source noteuspto-grants-2002_08