HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1504775Generated: October 30, 2026
Diisopropylethylamine → HCID 86731669, compound
https://huagongshe.com/reaction/1504775
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4-Chloro-6-methylpyridin-2-amine | HCID 19050509 | — |
| Reactant | HCID 178418936 | HCID 178418936 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86731669 | HCID 86731669 | — |
Reaction Steps
To 4-chloro-6-methylpyridin-2-amine (100 mg, 0.701 mmol) and 1,2,3-triazole (0.133 mL, 2.30 mmol) in a pressure tube was added DIPEA (0.185 mL, 1.06 mmol). The reaction mixture was sealed and heated at 150° C. for 1.5 hours. The reaction mixture was cooled, diluted with DCM (20 mL), and washed with water (10 mL). The organics were separated, dried over sodium sulfate, filtered, and concentrated under reduced pressure. The residue was slurried in 5% methanol/ethyl acetate (5 mL) and sonicated. The mixture was filtered, and the collected solids were dried under reduced pressure to afford 6-methyl-4-(1H-1,2,3-triazol-1-yl)pyridin-2-amine. MS ESI calc'd. for C8H10N5 [M+H]+ 176. found 176. 1H NMR (500 MHz, DMSO-d6) δ 8.79 (s, 1H), 7.95 (s, 1H), 6.90 (s, 1H), 6.75 (s, 1H), 6.28 (s, 2H), 2.23 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09216173B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-53c8f0429902452fbc9303e4becae7bb |
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| Source note | uspto-grants-2015_12 |
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