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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1669850Generated: November 2, 2026

Diisopropylethylamine → HCID 178488474, compound

https://huagongshe.com/reaction/1669850

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantHOAtHCID 181649—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantHCID 67335518HCID 67335518—
SolventDichloromethaneHCID 6344—
Solventdichloromethane N,N-dimethylformamideHCID 22350042—
ProductHCID 178488474HCID 178488474—

Reaction Steps

To a solution of the intermediate from example 73 step D (100 mg, 0.22 mmol) in 1:1 DMF/DCM (0.54 mL) was added 1-hydroxy-7-azabenzo-triazole (35 mg, 0.264 mmol), N,N-diisopropylethyl amine (92 μL, 0.53 mmol) amino methyl tetrazole (26 mg, 0.26 mmol) and 1-(3-(Dimethylamino)propyl-3-ethyl carbodiimide hydrochloride (51 mg, 0.26 mmol). The reaction was left stirring at room temperature for 18 hours. The reaction was diluted with DCM, washed with 1N HCl, dried over anhydrous Na2SO4, filtered and concentrated in vacuo. The residue was purified by reverse phase HPLC (Gilson) to give the title compound. 1H NMR (DMSO, 500 MHz): δ 9.21 (t, J=5.3 Hz, 1H), 7.88 (d, J=2.1 Hz, 2H), 7.83 (d, J=8.5 Hz, 2H), 7.56 (t, J=2.1 Hz, 1H), 7.39 (d, J=8.7 Hz, 2H), 7.15 (d, J=8.3 Hz, 2H), 7.12 (s, 1H), 7.04 (d, J=8.7 Hz, 2H), 5.49 (s, 2H), 4.74 (d, J=5.4 Hz, 2H), 3.79 (s, 3H). LC-MS: 3.82 min; (M+H)=534.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07989475B2
Source datasetuspto-grants-2011_08
ORD IDord-6dbca03a37454ef28fe4d60993c37a10
Source noteuspto-grants-2011_08