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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 243279Generated: October 29, 2026

Diisopropylethylamine → HCID 178423604, compound

https://huagongshe.com/reaction/243279

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant(S)-1-(4-Methyl-1-phenyl-1H-benzo[D]imidazol-2-YL)ethanamineHCID 68157022—
ReactantHCID 178478393HCID 178478393—
Solvent1-ButanolHCID 263—
ProductHCID 178423604HCID 178423604—

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of (S)-1-(4-methyl-1-phenyl-1H-benzoimidazol-2-yl)ethylamine from Example 3 (100 mg, 0.398 mmol), 6-chloro-9H-purine (68 mg, 0.438 mmol) and DIPEA (83 μL, 0.478 mmol) in n-butanol (1 mL) was stirred in a sealed vial at 100° C. for 20 h. After cooling to RT, the mixture was partitioned between DCM and water. The organic layer was then separated, dried and concentrated in vacuo. The resulting residue was purified by column chromatography (Si—PCC, gradient 0-10% 2M NH3/MeOH in DCM) and then sonicated in cyclohexane affording 108 as an off-white solid (56 mg, 38%) LCMS: RT 3.17 min [M+H]+ 370.1. 1H NMR (DMSO, 400 MHz): δ 8.13 (1H, bs), 8.08 (1H, s), 7.96-7.85 (1H, m), 7.67-7.44 (5H, m), 7.12-6.99 (2H, m), 6.86 (1H, d, J=7.80 Hz), 5.49 (1H, br), 2.56 (3H, s), 1.57 (3H, d, J=6.86 Hz)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653089B2
Source datasetuspto-grants-2014_02
ORD IDord-37375efb4e864dff9a715a06b3d684f4
Source noteuspto-grants-2014_02