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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1926440Generated: October 30, 2026

Hydrochloric Acid → HCID 44159051, compound

https://huagongshe.com/reaction/1926440

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
Reactant4-[4-[6-Amino-5-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)pyridin-3-yl]pyrazol-1-yl]piperidine-1-carboxylic acid tert-butyl esterHCID 53487960—
ReactantHCID 67521244HCID 67521244—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 44159051HCID 44159051—

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 4-{4-[6-amino-5-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-pyridin-3-yl]-pyrazol-1-yl}-piperidine-1-carboxylic acid tert-butyl ester (BB8) (30 mg, 0.064 mmol), 2-iodo-4,5,6,7-tetrahydrobenzothiazole (20 mg, 0.077 mmol), potassium carbonate (26 mg, 0.19 mmol), and Pd(PPh3)4 (7.4 mg, 0.0064 mmol) in DME (1.5 mL) and H2O (0.5 mL) was evacuated and refilled with N2 (3×). It was then heated at 100° C. for 30 min in the microwave reactor. The mixture was diluted with EtOAc (30 mL), washed with brine (10 mL), dried over anhydrous sodium sulfate, filtered, and concentrated in vacuo. The residue was purified by silica gel chromatography (Hex.:EtOAc=30:70→15:85) to give a yellow solid. This material was dissolved in DCM (2 mL) and treated with IM HCl in diethyl ether (3 mL). The resulting mixture was stirred at room temperature for 3 h. The title compound was collected by filtration as a yellow solid, washed with DCM, and dried in vacuo. 1H NMR (DMSO-d6, 400 MHz): δ=1.82-1.88 (m, 4H), 2.14-2.23 (m, 4H), 2.81-2.87 (m, 4H), 3.35-3.40 (m, 2H), 4.55 (mc, 1H), 8.09 (s, 1H), 8.44 (d, J=2.0 Hz, 1H), 8.47 (s, 1H), 8.50 (d, J=2.0 Hz, 1H). MS (ES+): m/z=381.17 [MH+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08178668B2
Source datasetuspto-grants-2012_05
ORD IDord-0f73bff4695b46f0acdd1794ff1fb09c
Source noteuspto-grants-2012_05