HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2426573Generated: November 1, 2026
Diisopropylethylamine → HCID 178452087, compound
https://huagongshe.com/reaction/2426573
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4-Amino-1-Boc-piperidine | HCID 1268291 | — |
| Reactant | HCID 178478393 | HCID 178478393 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 178452087 | HCID 178452087 | 36% |
Reaction Steps
A solution of 6-chloro-9H-purine (1.19 g, 7.68 mmol, 1.0 equiv; commercially available), 4-amino-piperidine-1-carboxylic acid tert-butyl ester (2.0 g, 10.0 mmol, 1.3 equiv) and N-ethyl diisopropylamine (3.0 mL, 2.3 g, 17.7 mmol, 2.3 equiv) in acetonitrile (16 mL) was heated by microwave irradiation to 160° C. for 20 min. The reaction mixture was concentrated under reduced pressure and the crude material purified by silica column chromatography using a MPLC system (CombiFlash Companion, Isco Inc.) eluting with a gradient of heptane/ethyl acetate. Suspension of the pre-purified material in ethyl acetate and filtration provided 0.89 g (36%) of the title compound. 1H NMR (300 MHz, DMSO): δ 1.31-1.43 (m, 2H), 1.40 (s, 9H), 1.87-1.90 (m, 2H), 2.74-2.88 (m, 2H), 3.92-3.96 (m, 2H), 4.32 (br s, 1H), 7.52 (br s, 1H), 8.08 (s, 1H), 8.18 (s, 1H). MS (ISP): 319.3 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07968568B2 |
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| Source dataset | uspto-grants-2011_06 |
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| ORD ID | ord-5f968dbfe8da4a1aa37e5fadc33fd8e4 |
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| Source note | uspto-grants-2011_06 |
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