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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2102237Generated: October 31, 2026

Diisopropylethylamine → HCID 178488473, compound

https://huagongshe.com/reaction/2102237

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantHOAtHCID 181649—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantPyBroPHCID 2733179—
ReactantHCID 67335518HCID 67335518—
ReactantHCID 178509299HCID 178509299—
SolventDichloromethaneHCID 6344—
Solventdichloromethane N,N-dimethylformamideHCID 22350042—
ProductHCID 178488473HCID 178488473—

Reaction Steps

To a solution of the intermediate from 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 tetrazole (56 mg, 0.66 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 checked by LC-MS and was found to have not gone to completion. An additional equivalent of amino tetrazole was added followed by Bromo-tris-pyrrolidino-phosphonium hexafluorophosphate (51 mg, 0.11 mmol). The reaction was complete in 3 hours. It was diluted with DCM (10 mL) and 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 8.04(d, J=8.5 Hz, 2H), 7.89(d, J=2.1 Hz, 2H), 7.56(t, J=1.9 Hz, 1H), 7.41(d, J=8.7 Hz, 2H), 7.21(d, J=8.4 Hz, 2H), 7.14(s, 1H), 7.05(d, J=8.7 Hz, 2H), 5.53(s, 2H), 3.79(s, 3H). LC-MS: 2.53 min; (M+H)=520.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07572922B2
Source datasetuspto-grants-2009_08
ORD IDord-5f90e1a26faf478ea1cdf567f2bd677b
Source noteuspto-grants-2009_08