Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1735473Generated: November 1, 2026

Ammonia → tert-Butyl 2,3-dihydro-1H,1'H-spiro[isoquinoline-4,4'-piperidine]-1'-carboxylate

https://huagongshe.com/reaction/1735473

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantMethanolHCID 887—
ReactantHCID 131719466HCID 131719466—
Producttert-Butyl 2,3-dihydro-1H,1'H-spiro[isoquinoline-4,4'-piperidine]-1'-carboxylateHCID 46942140—

Reaction Steps

The intermediate of Step A (100 mg) was stirred in methanol (2 mL) saturated with ammonia for one day, and evaporated to remove ammonia. The residue was redissolved in methanol (3 mL) and sodium cyanoborohydride (50 mg, excess) was added. The mixture was stirred overnight. Evaporation and purification gave the amine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05536716
Source datasetuspto-grants-1996_07
ORD IDord-c7995dcc25a54f9e8a92626ecf8355e7
Source noteuspto-grants-1996_07