HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2242911Generated: November 3, 2026
Diisopropylethylamine → HCID 11361581, compound
https://huagongshe.com/reaction/2242911
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Thiophene-3-sulfonyl Chloride | HCID 2776378 | — |
| Reactant | HCID 11817648 | HCID 11817648 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 11361581 | HCID 11361581 | — |
Reaction Steps
To a solution of 6-(3-amino-prop-1-ynyl)-2-furan-2-yl-[1,2,4]triazolo[1,5-a]pyrazin-8-ylamine (0.1 mmol, see Example 26 below) in THF (1 mL) was added thiophene-3-sulfonyl chloride (23.7 mg, 0.13 mmol), a catalytic quantity of DMAP and Hünig's base (52 uL, 0.3 mmol) successively. The reaction was stirred overnight and diluted with water. The aqueous layer was extracted with methylene chloride. The combined organic extracts were washed with brine and dried over magnesium sulfate. The solvent was then evaporated. The residue was purified using preparative HPLC (C18, H2O:MeCN gradient) to afford the desired product. 1H NMR (400 MHz, DMSO-d6) δ8.16 (1H), 8.09 (1H), 7.86 (1H), 7.68 (1H), 7.54 (1H), 7.31 (1H), 7.07(1H), 6.65 (1H), 4.23 (2H), 3.53 (d, J=7 Hz, 2H). MS: m/z 401 [M+1].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07674791B2 |
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| Source dataset | uspto-grants-2010_03 |
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| ORD ID | ord-e1c80ef601344a04853e3cce4bc97758 |
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| Source note | uspto-grants-2010_03 |
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