HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 522807Generated: October 29, 2026
Diisopropylethylamine → HCID 178461602, compound
https://huagongshe.com/reaction/522807
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | (3S)-3-Methylmorpholine--hydrogen chloride (1/1) | HCID 53486469 | — |
| Reactant | HCID 178461592 | HCID 178461592 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | (+-)-2-Butanol | HCID 6568 | — |
| Product | HCID 178461602 | HCID 178461602 | 66% |
Reaction Steps
2-Chloro-6-((R)-3-methyl-morpholin-4-yl)-9H-purine (712 mg, 2.81 mmol), diisopropylethylamine (0.98 mL, 5.61 mmol), and (S)-3-methylmorpholin hydrochloride (579 mg, 4.21 mmol) were stirred in 2-butanol (3 mL) in a closed 5 mL microwave tube under argon at 50° C., until all ingredients were dissolved. The reaction was then stirred at 175° C. for 48 hours. The organic layer was diluted with 200 mL of CH2Cl2 and washed with brine. Drying over Na2SO4, filtering and concentration under reduced pressure gave a residue, which was purified by column chromatography (40 g SiO2, CH2Cl2/EtOH/aq NH3 in a gradient from 100/0/0.1 to 90/10/0.1) to give the product as a solid (588 mg, 66%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09334271B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-695a09cf50ac47d7a23b94020bd86545 |
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| Source note | uspto-grants-2016_05 |
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