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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1397010Generated: October 30, 2026

Tert-butyl (piperidin-4-ylmethyl)carbamate → HCID 86672840, compound

https://huagongshe.com/reaction/1397010

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl (piperidin-4-ylmethyl)carbamateHCID 723429—
ReactantHCID 86672841HCID 86672841—
ProductHCID 86672840HCID 86672840—

Reaction Steps

(Z)-5-((6-(4-(aminomethyl)piperidin-1-yl)pyrimidin-4-yl)methylene)thiazolidine-2,4-dione was prepared using the general reductive amination procedure, (Z)-5-((2-(methylsulfonyl)pyrimidin-4-yl)methylene)-3-(2-(pyridin-2-yl)ethyl)thiazolidine-2,4-dione, and tert-butyl(piperidin-4-ylmethyl)carbamate followed by the general de-protection procedure (16 mg, 30.6 mg theoretical, 52.3%). LC-MS m/z 425.5 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901145B2
Source datasetuspto-grants-2014_12
ORD IDord-bff8a679fc674ed1863d5eb833f8ec64
Source noteuspto-grants-2014_12