HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 539901Generated: October 26, 2026
Hydrochloric Acid → HCID 86698991, compound
https://huagongshe.com/reaction/539901
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 1-methyl-1H-indazol-5-amine | HCID 2768032 | — |
| Reactant | 2-Chloro-4-(methylthio)pyrimidine | HCID 16427148 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 86698991 | HCID 86698991 | — |
Reaction Steps
To a solution of 2-chloro-4-(methylthio)pyrimidine (1.0 g, 6.2 mmol) and 1-methyl-1H-indazol-5-amine (1.0 g, 6.8 mmol) in 10 mL of ethanol was added 1 mL of concentrated hydrochloric acid at room temperature. The reaction mixture was heated at 80° C. for 5 hours with monitoring a reaction with LC-MS or thin layer chromatography (TLC). The reaction mixture was cooled to room temperature to form a solid. The resulting solid was collected by filtration and rinsed with cold ethanol to afford 1-methyl-N-(4-(methylthio)pyrimidin-2-yl)-1H-indazol-5-amine, intermediate 11 (0.7 g, 41%). The resulting solid was dissolved in 20 mL of dichloromethane and treated with m-chloroperbenzoic acid (mCPBA, 0.9 g, 5.2 mmol) at room temperature. After being stirred for 12 hours at room temperature, the reaction mixture was extracted with dichloromethane (×3) and washed with brine. The collected organic layer was dried over anhydrous sodium sulfate and then concentrated in vacuo. The resulting solid was slurrified with heptane and then collected by filtration to afford the desired intermediate 12 as a white solid (0.6 g, 77%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08871778B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-63cc732551294189b17ebd8ffdea199f |
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| Source note | uspto-grants-2014_10 |
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