HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 528036Generated: October 25, 2026
6-chloro-N4-methylpyrimidine-4,5-diamine → 6-Chloro-8-(1-ethyl-1H-pyrazol-4-yl)-9-methyl-9H-purine
https://huagongshe.com/reaction/528036
Participants
| Role | Name | HCID | Charge |
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| Reactant | 6-chloro-N4-methylpyrimidine-4,5-diamine | HCID 308477 | — |
| Reactant | 1-Ethyl-1H-pyrazole-4-carboxaldehyde | HCID 2758900 | — |
| Catalyst | Trichloroiron;hexahydrate | HCID 16211236 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 6-Chloro-8-(1-ethyl-1H-pyrazol-4-yl)-9-methyl-9H-purine | HCID 86711712 | 103% |
Reaction Steps
To a solution of 6-chloro-N4-methylpyrimidine-4,5-diamine (300 mg, 1.9 mmol) in anhydrous DMF (8 mL) were added 1-ethyl-1H-pyrazole-4-carbaldehyde (236 mg, 1.9 mmol) and Iron (III) chloride hexahydrate (0.51 g, 1.9 mmol). The dark brown solution was heated to 90° C. for 14 hour in an open air vessel. The reaction mixture was cooled to room temperature and poured over ice (20 g). The resulting precipitate was collected by vacuum filtration, and triturated with 10 mL of ethanol at 50° C. for 30 min. The solids were collected by vacuum filtration to give 514 mg of the title compound. 1H NMR (400 MHz, DMSO-d6): δ 8.66 (t, 2H), 8.19 (s, 1H), 4.25 (q, 2H), 3.95 (s, 3H), 1.43 (t, 3H); MS (EI) for C11H11ClN6: 263.3 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09346807B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-9c63682f68d14f359ca1087139334be9 |
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| Source note | uspto-grants-2016_05 |
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