HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1364567Generated: October 29, 2026
Diisopropylethylamine → HCID 66920760, compound
https://huagongshe.com/reaction/1364567
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 | 5-(Aminomethyl)-1,3-thiazole | HCID 5304077 | — |
| Reactant | 4-Amino-5-cyano-6-ethoxypicolinic acid | HCID 11846460 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | HCID 66920760 | HCID 66920760 | — |
Reaction Steps
In a 20 mL vial a solution of Example 104A (32.5 mg, 0.16 mmol) dissolved in N,N-dimethylacetamide (0.8 mL) was added, followed by the addition of O-benzotriazol-1-yl-N,N,N′,N′-tetramethyluronium tetrafluoroborate (50.4 mg, 0.16 mmol) dissolved in N,N-dimethylacetamide (0.8 mL). Then, 5-(aminomethyl)thiazole (21.7 mg, 0.19 mmol) dissolved in N,N-dimethylacetamide (0.6 mL) was added followed by the addition of diisopropyl ethyl amine (57.9 uL, 0.31 mmol) dissolved in N,N-dimethylacetamide (0.8 mL). The mixture was shaken at room temperature overnight. The reaction was checked by LC/MS and concentrated to dryness. The residue was dissolved in 1:1 dimethyl sulfoxide/methanol and purified by reverse phase HPLC (0-70% CH3CN in 10 mM aq. ammonium acetate) to give the titled compound. 1H NMR (500 MHz, DMSO-d6) δ ppm 1.25-1.39 (m, 3H) 4.43-4.54 (m, 2H) 4.58-4.68 (m, 2H) 7.04-7.14 (m, 1H) 7.37-7.45 (m, 1H) 8.83-9.19 (m, 1H); MS (ESI) positive ion 304 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07888374B2 |
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| Source dataset | uspto-grants-2011_02 |
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| ORD ID | ord-2c7f9e82d48f4bea9289d88484b3f451 |
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| Source note | uspto-grants-2011_02 |
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