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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1398580Generated: October 26, 2026

Thionyl Chloride → 1-{[1-(2-Aminopyrimidin-4-yl)-6-bromoindazol-3-yl]carbonyl}azetidin-3-ol

https://huagongshe.com/reaction/1398580

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantDiisopropylethylamineHCID 81531—
Reactant3-Hydroxyazetidine hydrochlorideHCID 2759290—
Reactant1-(2-Aminopyrimidin-4-yl)-6-bromoindazole-3-carboxylic acidHCID 68181966—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product1-{[1-(2-Aminopyrimidin-4-yl)-6-bromoindazol-3-yl]carbonyl}azetidin-3-olHCID 6818179449.1%

Reaction Conditions

Temperature40 °C

Reaction Steps

To a solution of 1-(2-aminopyrimidin-4-yl)-6-bromoindazole-3-carboxylic acid (0.38 g, 1.12 mmol)) in DCM (5 mL), was added thionyl chloride (0.49 ml, 6.74 mmol) followed by a drop of DMF. The mixture was stirred at 40° C. overnight. The reaction mixture was concentrated in vacuo and DCM added and the concentration repeated (×2). The acid chloride intermediate was suspended in DCM (10 ml), azetidin-3-ol hydrochloride (491.82 mg, 4.49 mmol) followed by DIPEA (0.86 ml, 4.94 mmol). The reaction was stirred at RT for 0.5 hr and then concentrated in vacuo. The residue was diluted with more DCM and water and the organics extracted (2×20 ml DCM). The combined organic layers were dried (Na2SO4), filtered and concentrated in vacuo to give the title intermediate (214 mg, LC-MS purity=63%); LC-MS: m/z=+388.95/390.80 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901313B2
Source datasetuspto-grants-2014_12
ORD IDord-f7178482e88b4e2eaed03f9971c62a18
Source noteuspto-grants-2014_12