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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 705154Generated: October 29, 2026

HCID 178452634, compound → HCID 178512234, compound

https://huagongshe.com/reaction/705154

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 178452634HCID 178452634—
CatalystHCID 178506449HCID 178506449—
SolventIsopropanolHCID 3776—
ProductHCID 178512234HCID 178512234—

Reaction Steps

The single enantiomer was then BOC-protected, the nitro group reduced by treatment with H2/Pd and the primary aniline treated with diphenyl cyanocarboimidate (slight excess) in 20 mL of isopropanol with stirring at ambient temperature overnight. The solid was filtered, washed with isopropanol and ether and dried to give phenyl (7S) N′-cyano-N-(7-amino-6,7,8,9-tetrahydro-5H-benzo[7]annulene-2-yl)carbamimidate, as a white solid in high yield (from the single enantiomer via transamination).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09173882B2
Source datasetuspto-grants-2015_11
ORD IDord-e0ff593626f94e8b91b655a5a260e729
Source noteuspto-grants-2015_11