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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 877544Generated: October 30, 2026

3-Hydroxypiperidine → HCID 89689614, compound

https://huagongshe.com/reaction/877544

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-HydroxypiperidineHCID 23293—
ReactantDiisopropylethylamineHCID 81531—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
ReactantHCID 89689766HCID 89689766—
SolventDimethylformamideHCID 6228—
ProductHCID 89689614HCID 89689614—

Reaction Steps

The 2-(6-chloro-4-(isopropylamino)pyridin-3-yl)thiazole-4-carboxylic acid (23a) (100 mg, 0.336 mmol) was dissolved in DMF (5 mL), piperidin-3-ol (1.679 mmol) was added and stirred at room temperature. Added DIPEA (1.343 mmol), followed by addition of HATU (1.008 mmol) and stirred for 3 h. The reaction mixture was concentrated under reduced pressure to remove excess of DMF. The residue obtained was partitioned between water and EtOAc. The organic layer was separated, dried over Na2SO4, filtered and concentrated. The crude material obtained was purified by column chromatography through silica gel and MeOH: CHCl3 as eluent to afford the title compound, (2-(6-chloro-4-(isopropylamino)pyridin-3-yl)thiazol-4-yl)(3-hydroxypiperidin-1-yl)methanone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08987311B2
Source datasetuspto-grants-2015_03
ORD IDord-d709d117001b4f49979df6ffcf45edb6
Source noteuspto-grants-2015_03