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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2092966Generated: November 1, 2026

Diisopropylethylamine → HCID 51354790, compound

https://huagongshe.com/reaction/2092966

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantPyBOPHCID 2724699—
Reactant4,4-Difluoropiperidine hydrochlorideHCID 2758351—
ReactantHCID 58227488HCID 58227488—
SolventDichloromethaneHCID 6344—
ProductHCID 51354790HCID 5135479092.8%

Reaction Steps

In a small culture tube, 2-phenylethynyl-thiazole-5-carboxylic acid (28 mg, 0.12 mmol) [Intermediate 1], 4,4-difluoropiperidine hydrochloride (23 mg, 0.14 mmol) (Oakwood Products, Inc. (West Columbia, S.C., USA) and dichloromethane (1.5 mL) were added. To the mixture, PyBOP® (76 mg, 0.14 mmol) was added, followed by N,N-diisopropylethylamine (63 μL, 0.36 mmol), and the reaction was stirred at room temperature for about 17 hours. Afterwards, the crude reaction mixture was directly purified by Preparative TLC, eluting with 40% EtOAc in hexanes to give 37 mg (92%) of the titled compound, (4,4-difluoro-piperidin-1-yl)-(2-phenylethynyl-thiazol-5-yl)-methanone, as a white solid. 1H NMR (300 MHz, CDCl3) δ 7.99 (s, 1H), 7.66-7.59 (m, 2H), 7.49-7.37 (m, 3H), 3.92-3.82 (m, 4H), 2.18-2.01 (m, 4H). LC/MS (Method 3), RT=1.43 min. Calculated [M+H]+=333; Observed [M+H]+=333.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08440837B2
Source datasetuspto-grants-2013_05
ORD IDord-b6953dd68a2048948f0ee09361dc14d7
Source noteuspto-grants-2013_05