HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1014957Generated: October 31, 2026
Diisopropylethylamine → HCID 178463182, compound
https://huagongshe.com/reaction/1014957
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2,6-Dichloro-9-(tetrahydro-2H-pyran-2-yl)-9H-purine | HCID 270265 | — |
| Reactant | HCID 178463186 | HCID 178463186 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 178463182 | HCID 178463182 | 91.8% |
Reaction Steps
(2R,3R,4R,5R)-2-{6-[(trans-4-Aminocyclohexyl)amino]-2-chloro-9H-purin-9-yl}-5-(2-ethyl-2H-tetrazol-5-yl)tetrahydrofuran-3,4-diyl diacetate (Intermediate 4) (7.9 g) was dissolved in isopropanol (200 ml) and stirred at room temperature under nitrogen. N,N-diisopropylethylamine (10 ml) was added followed by 2,6-dichloro-9-(tetrahydro-2H-pyran-2-yl)-9H-purine (3.92 g). The mixture was stirred at 60° C. under nitrogen for 18 h. The reaction mixture was allowed to cool to room temperature and evaporated down in vacuo. The residue was partitioned between ethyl acetate and water. The organic phase was separated and the aqueous extracted twice with ethyl acetate. The organic phases were combined, dried (MgSO4), and evaporated down in vacuo to give the title compound (10.35 g). Used without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07985740B2 |
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| Source dataset | uspto-grants-2011_07 |
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| ORD ID | ord-e601ac6747994d42b2b1e22fabd4c5c1 |
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| Source note | uspto-grants-2011_07 |
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