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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2038763Generated: November 2, 2026

Potassium Phosphate, Tribasic → 2-Methyl-propane-2-sulfinic acid{1-[6-(6-hydroxymethyl-pyridin-3-yl)-pyridazin-3-yl]-1-methyl-ethyl}-amide

https://huagongshe.com/reaction/2038763

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant6-(Hydroxymethyl)pyridine-3-boronic acidHCID 44118255—
Reactant2-Methyl-propane-2-sulfinic acid[1-(6-chloro-pyridazin-3-yl)-1-methyl-ethyl]-amideHCID 88959179—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventDimethoxyethane ethanol waterHCID 86587095—
Product2-Methyl-propane-2-sulfinic acid{1-[6-(6-hydroxymethyl-pyridin-3-yl)-pyridazin-3-yl]-1-methyl-ethyl}-amideHCID 6837896921.3%

Reaction Conditions

Temperature140 °C

Reaction Steps

Impure 2-methyl-propane-2-sulfinic acid[1-(6-chloro-pyridazin-3-yl)-1-methyl-ethyl]-amide (15 mg, 0.054 mmol) was combined with Pd(dppf)Cl2.dichloromethane complex (4.7 mg, 0.006 mmol), 1M K3PO4 (0.07 mL, 0.07 mmol) and 2-(hydroxymethyl)pyridine-5-boronic acid (18 mg, 0.12 mmol) in a microwave vial. A 7:3:2 mixture of DME/H2O/EtOH (1 mL) was added. The vial was flushed with argon and sealed. This vial was then heated in the microwave reactor for 15 min at 140° C. The reaction mixture was diluted with 2 mL of water and extracted 4×4 mL with EtOAc. The combined organic layers were dried over MgSO4, filtered and concentrated. Purification via normal phase flash chromatography on silica gel (0→4% MeOH/CH2Cl2) yielded 4 mg of 2-methyl-propane-2-sulfinic acid{1-[6-(6-hydroxymethyl-pyridin-3-yl)-pyridazin-3-yl]-1-methyl-ethyl}-amide as a brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08575360B2
Source datasetuspto-grants-2013_11
ORD IDord-a989d63ffde34ae1b1bc49a86a35fa15
Source noteuspto-grants-2013_11