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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2200016Generated: November 3, 2026

Water → (S)-2-Methyl-piperidine-1-carboxylic acid N'-(5-fluoro-pyridin-2-yl)-hydrazide

https://huagongshe.com/reaction/2200016

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDiisopropylethylamineHCID 81531—
Reactant5-Fluoro-2-hydrazinylpyridineHCID 19916786—
Reactant(2S)-2-Methylpiperidine-1-carbonyl chlorideHCID 45081356—
SolventDichloromethaneHCID 6344—
SolventDiethylether pentaneHCID 21877078—
Product(S)-2-Methyl-piperidine-1-carboxylic acid N'-(5-fluoro-pyridin-2-yl)-hydrazideHCID 8668710477.8%

Reaction Steps

A stirred solution of Intermediate 2b (17.20 g, assumed to be 95.49 mmol) and (5-fluoro-pyridin-2-yl)-hydrazine (12.14 g, 95.51 mmol) in DCM (300 mL) at RT was treated with DIPEA (34 mL, 195.18 mmol) during 5 min. This mixture was continued to be stirred at RT for 4 days before being added to water (500 mL) and phases separated. The aqueous layer was further extracted into DCM (4×100 mL), combined extracts washed with brine, dried (MgSO4), passed through a phase separation cartridge and concentrated in vacuo to give a residual solid. This product was treated with Et2O-pentane and the resultant solids filtered off and dried to give Intermediate 2c (18.74 g, 77%). LCMS (Method 3) Rt 2.26 min, m/z 253 [MH+]. 1H NMR (300 MHz, CDCl3): 1.23 (3H, d, J 6.9), 1.40-1.74 (6H, m), 2.97 (1H, td, J 13.1, 3.0), 3.82-3.91 (1H, m), 4.27-4.38 (1H, m), 6.54 (1H, s), 6.78 (1H, ddd, J 9.1, 3.7, 0.6), 7.30 (1H, ddd, J 9.1, 7.8, 2.9), 8.00 (1H, d, J 2.6).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09359354B2
Source datasetuspto-grants-2016_06
ORD IDord-fea1acf6cdb64699bd8b3113a5fc66d6
Source noteuspto-grants-2016_06