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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 3-Hydroxyazetidine hydrochloride | HCID 2759290 | — |
| Reactant | 1-(2-Aminopyrimidin-4-yl)-6-bromoindazole-3-carboxylic acid | HCID 68181966 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-{[1-(2-Aminopyrimidin-4-yl)-6-bromoindazol-3-yl]carbonyl}azetidin-3-ol | HCID 68181794 | 49.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08901313B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-f7178482e88b4e2eaed03f9971c62a18 |
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| Source note | uspto-grants-2014_12 |
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