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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 243280Generated: October 30, 2026

Diisopropylethylamine → HCID 178423603, compound

https://huagongshe.com/reaction/243280

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant(1R)-1-(4-Methyl-1-phenyl-1H-benzimidazol-2-yl)ethan-1-amineHCID 68157262—
ReactantHCID 178478393HCID 178478393—
Solvent1-ButanolHCID 263—
ProductHCID 178423603HCID 178423603—

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of (R)-1-(4-methyl-1-phenyl-1H-benzoimidazol-2-yl)ethylamine from Example 2 (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 109 as a brown solid (62 mg, 42%) LCMS: RT 3.17 min [M+H]+ 370.1. 1H NMR (DMSO, 400 MHz): δ 8.18-8.06 (2H, m), 7.95-7.86 (1H, m), 7.66-7.45 (5H, m), 7.11-7.00 (2H, m), 6.86 (1H, d, J=7.81 Hz), 5.49 (1H, br), 2.56 (3H, s), 1.57 (3H, d, J=6.84 Hz)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653089B2
Source datasetuspto-grants-2014_02
ORD IDord-74a4417170694a23aae4502d87db66f3
Source noteuspto-grants-2014_02