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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1500352Generated: October 30, 2026

Diphenyl N-Cyanocarbonimidate → HCID 178512234, compound

https://huagongshe.com/reaction/1500352

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiphenyl N-CyanocarbonimidateHCID 688090—
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 cyanocarbonimidate (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 numberUS09206161B2
Source datasetuspto-grants-2015_12
ORD IDord-bac8a748b96c477a93855a46d68e18da
Source noteuspto-grants-2015_12