HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 509915Generated: November 3, 2026
Diisopropylethylamine → HCID 117856350, compound
https://huagongshe.com/reaction/509915
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate | HCID 2733207 | — |
| Reactant | 3,5-Diamino-6-chloro-pyrazine acid | HCID 6452119 | — |
| Reactant | HCID 131733252 | HCID 131733252 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 117856350 | HCID 117856350 | — |
Reaction Steps
A solution of 3,5-diamino-6-chloropyrazine-2-carboxylic-acid (Intermediate 1.1.1, 46 mg, 0.25 mmol), 3-amino-1-ethoxycarbonylmethyl-1-[3-(4-methoxy-phenyl)-propyl]-piperidinium bromide trifluoroacetate salt (Intermediate 3.1.2, 230 mg, 0.25 mmol), O-(benzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium tetrafluoroborate (86 mg, 0.27 mmol) and N,N-diisopropylethylamine (0.15 mL, 0.1 mmol) in dry N,N-dimethylformamide (5 mL) is stirred for 5 hours at room temperature. The solution is concentrated under reduced pressure to half of the volume, water (2 mL) added and the mixture purified via preparative reverse phase HPLC (gradient of acetonitrile in water+0.05% trifluoroacetic acid). Fractions containing the title compound are concentrated under reduced pressure. The residue is treated with HCl in diethyl ether (2 M, 2 mL), the solvent removed and the residue dried at 50° C. under vacuum. Yield: 56 mg. IC50=0.15.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09096548B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-a3a5e5c9a2dd48328160d8f249c6d336 |
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| Source note | uspto-grants-2015_08 |
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