HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1872029Generated: November 3, 2026
Morpholine → 4-(2-chloro-6-methylpyrimidin-4-yl)morpholine
https://huagongshe.com/reaction/1872029
Participants
| Role | Name | HCID | Charge |
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| Reactant | Morpholine | HCID 8083 | — |
| Reactant | 2,4-Dichloro-6-methylpyrimidine | HCID 79471 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-(2-chloro-6-methylpyrimidin-4-yl)morpholine | HCID 3156999 | 72.5% |
Reaction Steps
Part A: A mixture of 2,4-dichloro-6-methylpyrimidine (4 g, 24.54 mmoles), morpholine (2.14 mL, 24.54 mmoles) and N,N-diisopropylethylamine (4.52 mL) in ethanol (60 mL) was stirred at 0° C. for 3 hours, 25° C. for 24 hours, followed by reflux for 1 hour. The solvent was removed under vacuum and the residue was partitioned between ethyl acetate (200 mL) and aq. sodium hydroxide (1 M, 50 mL). The organic layer was washed with water and brine and dried and concentrated in vacuo. The residue was recrystallized from ethyl acetate/hexanes to give 2-chloro-4-morpholino-6-methylpyrimidine (3.8 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06107301 |
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| Source dataset | uspto-grants-2000_08 |
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| ORD ID | ord-9891d888db7e40beb4876e2a26d55331 |
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| Source note | uspto-grants-2000_08 |
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