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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1913818Generated: November 1, 2026

N-((S)-6-Pyridin-3-yl-1,2,3,4-tetrahydronaphthalen-2-yl)-4-[(S)-1-(tetrahydrofuran-2-yl)methoxy]benzamide → N-((S)-6-Piperidin-3-yl-1,2,3,4-tetrahydronaphthalen-2-yl)-4-[(S)-1-(tetrahydrofuran-2-yl)methoxy]benzamide

https://huagongshe.com/reaction/1913818

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-((S)-6-Pyridin-3-yl-1,2,3,4-tetrahydronaphthalen-2-yl)-4-[(S)-1-(tetrahydrofuran-2-yl)methoxy]benzamideHCID 67544347—
CatalystAdams' catalystHCID 345198—
SolventAcetic AcidHCID 176—
ProductN-((S)-6-Piperidin-3-yl-1,2,3,4-tetrahydronaphthalen-2-yl)-4-[(S)-1-(tetrahydrofuran-2-yl)methoxy]benzamideHCID 59505834—

Reaction Steps

A mixture of N-((S)-6-pyridin-3-yl-1,2,3,4-tetrahydronaphthalen-2-yl)-4-[(S)-1-(tetrahydrofuran-2-yl)methoxy]benzamide (0.60 g), glacial acetic acid (30 ml) and platinum(IV) oxide (0.10 g) was stirred vigorously under a hydrogen atmosphere (balloon) for 12 hours. The catalyst was filtered off with suction and the filtrate was concentrated. The product was thus obtained with the molecular weight of 434.58 (C27H34N2O3); MS (ESI): 435 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08609731B2
Source datasetuspto-grants-2013_12
ORD IDord-846485c8493d4c1fb2d8e70fc1dde47d
Source noteuspto-grants-2013_12