HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2102241Generated: October 29, 2026
Diisopropylethylamine → HCID 178488472, compound
https://huagongshe.com/reaction/2102241
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HOAt | HCID 181649 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | HCID 67337219 | HCID 67337219 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | dichloromethane N,N-dimethylformamide | HCID 22350042 | — |
| Product | HCID 178488472 | HCID 178488472 | — |
Reaction Steps
To a solution of the intermediate from example 76 step A (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 ethyl acetate, 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 9.22(t, J=5.5 Hz, 1H), 7.84(d, J=8.5 Hz, 2H), 7.79(d, J=8.9 Hz, 2H), 7.69(t, J=1.9 Hz, 1H), 7.54(d, J=1.8 Hz, 2H), 7.17(d, J=8.2 Hz, 2H), 7.06(s, 1H), 7.0(d, J=8.7 Hz, 2H), 5.53(s, 2H), 4.74(d, J=5.5 Hz, 2H), 3.79(s, 3H). LC-MS: 2.32 min; (M+H)=534.3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07572922B2 |
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| Source dataset | uspto-grants-2009_08 |
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| ORD ID | ord-b9cc9d682bcf46ada1444126372cbbaa |
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| Source note | uspto-grants-2009_08 |
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