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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 244608Generated: October 29, 2026

HCID 178452634, compound → HCID 178512234, compound

https://huagongshe.com/reaction/244608

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 (7 S)—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 numberUS08658669B2
Source datasetuspto-grants-2014_02
ORD IDord-ce9984e4ef85422f87e777b401e82f5d
Source noteuspto-grants-2014_02