HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 594062Generated: October 25, 2026
Triethylamine → 4-(6-Chloro-2-morpholinopyrimidin-4-yl)-2,2-dimethylmorpholine
https://huagongshe.com/reaction/594062
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-(4,6-Dichloropyrimidin-2-yl)morpholine | HCID 2772068 | — |
| Reactant | 2,2-Dimethylmorpholine | HCID 18959674 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-(6-Chloro-2-morpholinopyrimidin-4-yl)-2,2-dimethylmorpholine | HCID 90409549 | — |
Reaction Steps
A mixture of 2,2-dimethylmorpholine (2.0 equiv.), 4-(4,6-dichloropyrimidin-2-yl)morpholine (1 equiv.) and triethylamine (6 equiv.) in EtOH (0.2 M) were heated to 110° C. for 25 min in the microwave. The reaction mixture was partitioned between EtOAc and water. The organic phase was dried over sodium sulfate. The resulting solution was concentrated and dried under vacuo to give 4-(6-chloro-2-morpholinopyrimidin-4-yl)-2,2-dimethylmorpholine and was used in the next step without further purification. LCMS (m/z) (M+H)=313.2, Rt=0.86 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09242969B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-4511474057dd4666a0129689127ff48e |
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| Source note | uspto-grants-2016_01 |
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