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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 243486Generated: October 30, 2026

Diisopropylethylamine → HCID 178462636, compound

https://huagongshe.com/reaction/243486

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant6-chloro-9-(tetrahydro-2H-pyran-2-yl)-9H-purineHCID 97740—
ReactantHCID 68157537HCID 68157537—
ProductHCID 178462636HCID 17846263631.1%

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture of (S)-1-(1-ethyl-6-fluoro-7-pyridin-2-yl-1H-benzoimidazol-2-yl)ethylamine (0.203 g, 0.715 mmol), 6-chloro-9-(tetrahydropyran-2-yl)-9H-purine (145 mg, 0.60 mmol) and DIPEA (543 μL, 3.0 mmol) were added and the reaction mixture heated at 90° C. for 16 hours. The reaction mixture was loaded onto an SCX column to remove the THP group. The column was washed with MeOH and the product was eluted with 2M NH3 in MeOH. The product fractions were collected, concentrated in vacuo and the resultant residue was subjected to flash chromatography (Si—PPC, gradient 0-7% MeOH in DCM) to give 412 as a white solid (75 mg, 25%). LCMS (Method K): RT 2.76 min [M+H]+ 403. 1H NMR (DMSO, 400 MHz): δ 12.83 (1H, br s), 8.68 (1H, d, J=4.8 Hz), 8.12 (2H, d, J=14.3 Hz), 7.95 (1H, br s), 7.91 (1H, td, J=7.7, 1.7 Hz), 7.68-7.62 (2H, m), 7.46 (1H, d, J=7.2, 5.0 Hz), 7.11 (1H, dd, J=10.4, 9.0 Hz), 5.78-5.67 (1H, m), 3.91-3.71 (2H, m), 1.63 (3H, d, J=6.8 Hz), 0.71 (3H, t, J=6.9 Hz)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653089B2
Source datasetuspto-grants-2014_02
ORD IDord-514677035c9744099c0eb2c7cf8708b4
Source noteuspto-grants-2014_02