HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2176867Generated: October 31, 2026
Ethanol → 6-chloro-N-methylpyrimidin-4-amine
https://huagongshe.com/reaction/2176867
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanol | HCID 702 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | 4,6-Dichloropyrimidine | HCID 70943 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 6-chloro-N-methylpyrimidin-4-amine | HCID 309479 | — |
Reaction Steps
This material was prepared by a modified procedure published in the literature (J. Appl. Chem. 1955, 5, 358): To a suspension of commercially available 4,6-dichloropyrimidine (20 g, 131.6 mmol, 1.0 eq.) in isopropanol (60 ml) is added 33% methylamine in ethanol (40.1 ml, 328.9 mmol, 2.5 eq.) at such a rate that the internal temperature does not rise above 50° C. After completion of the addition the reaction mixture was stirred for 1 h at room temperature. Then, water (50 ml) is added and the suspension formed is chilled in an ice bath to 5° C. The precipitated product is filtered off, washed with cold isopropanol/water 2:1 (45 ml) and water. The collected material is vacuum dried over night at 45° C. to afford the title compound as colorless powder: tR=3.57 min (purity: >99%, gradient A), ESI-MS: 144.3/146.2 [MH]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09067896B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-c305227401094963bc5ca0f8a96825ee |
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| Source note | uspto-grants-2015_06 |
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