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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2426573Generated: November 1, 2026

Diisopropylethylamine → HCID 178452087, compound

https://huagongshe.com/reaction/2426573

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant4-Amino-1-Boc-piperidineHCID 1268291—
ReactantHCID 178478393HCID 178478393—
SolventAcetonitrileHCID 6342—
ProductHCID 178452087HCID 17845208736%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07968568B2
Source datasetuspto-grants-2011_06
ORD IDord-5f968dbfe8da4a1aa37e5fadc33fd8e4
Source noteuspto-grants-2011_06