HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 607444Generated: October 29, 2026
N,N-Diethylethylenediamine → HCID 57657887, compound
https://huagongshe.com/reaction/607444
Participants
| Role | Name | HCID | Charge |
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| Reactant | N,N-Diethylethylenediamine | HCID 60993 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphate | HCID 151348 | — |
| Reactant | 3-[N-({5-[(3-{[(1,3-dimethyl-1H-pyrazol-5-yl)carbonyl]amino}phenyl)ethynyl]pyridin-3-yl}carbonyl)-S-methylsulfonimidoyl]benzoic acid | HCID 57657927 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 57657887 | HCID 57657887 | — |
Reaction Steps
To a solution of 3-[N-({5-[(3-{[(1,3-dimethyl-1H-pyrazol-5-yl)carbonyl]amino}phenyl)ethynyl]pyridin-3-yl}carbonyl)-S-methylsulfonimidoyl]benzoic acid (52 mg, 0.096 mmol), 2-diethylaminoethylamine (0.016 ml, 0.115 mmol), and N,N-diisopropylethylamine (0.034 ml, 0.192 mmol) in 3.0 ml DMF at room temperature was added benzotriazole-1-yl-oxy-tris-(dimethylamino)-phosphoniumhexafluorophosphate (47 mg, 0.106 mmol). The reaction was stirred at room temperature for 1.5 hours, and then partitioned between EtOAc and dilute brine. The EtOAc layer was washed with saturated NaHCO3 solution, dilute brine, dried with anhydrous Na2SO4 and rotary evaporated. The yellow oil (combined 7 mg impure product from another lot) was chromatographed eluting with EtOAc/MeOH, then rechromatographed using a preparative TLC plate (eluted with (1:1:2.5) CHCl3:EtOAc:MeOH plus NH4OH) to give the title compound as a white solid foam (28 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07915443B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-d6188d6b21714b7dbcb0dea053a314ae |
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| Source note | uspto-grants-2011_03 |
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