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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2370521Generated: October 28, 2026

tert-butyl (3S)-3-aminopiperidine-1-carboxylate → HCID 57725419, compound

https://huagongshe.com/reaction/2370521

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-butyl (3S)-3-aminopiperidine-1-carboxylateHCID 1501975—
Reactant2-Pyridinecarboxamide, N-methyl-4-[[2-(methylsulfinyl)-6-benzothiazolyl]oxy]-HCID 57725393—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 57725419HCID 5772541940%

Reaction Conditions

Temperature105 °C

Reaction Steps

To the solution of N-methyl-4-(2-(methylsulfinyl)benzo[d]thiazol-6-yloxy)picolinamide (104 mg, 0.3 mmol) in 2 ml of NMP was added (S)-tert-butyl 3-aminopiperidine-1-carboxylate (240 mg, 1.2 mmol). The reaction solution was stirred at 105° C. for 5 days. The crude reaction solution was purified on prep HPLC and evaporated in vaccuo to give (S)-tert-butyl 3-(6-(2-(methylcarbamoyl)pyridin-4-yloxy)benzo[d]thiazol-2-ylamino)piperidine-1-carboxylate (56 mg, 0.12 mmol) as white powder. ES/MS m/z 484.2 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08710048B2
Source datasetuspto-grants-2014_04
ORD IDord-d424ca7168e54e21ac88e4682bca1712
Source noteuspto-grants-2014_04