HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1523059Generated: October 30, 2026
Dimethylamine → 5-Chloro-3-(2-(6-ethynylpyridin-2-yl)-2-oxoethyl)-3-hydroxy-1-propylindolin-2-one
https://huagongshe.com/reaction/1523059
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylamine | HCID 674 | — |
| Reactant | 5-Chloro-1-propylindoline-2,3-dione | HCID 2988281 | — |
| Reactant | 1-(6-((Trimethylsilyl)ethynyl)pyridin-2-yl)ethan-1-one | HCID 11680135 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 5-Chloro-3-(2-(6-ethynylpyridin-2-yl)-2-oxoethyl)-3-hydroxy-1-propylindolin-2-one | HCID 86300243 | — |
Reaction Steps
To a clean biotage vial equipped with a stir bar was added 1-(6-((trimethylsilyl)ethynyl)pyridin-2-yl)ethanone (0.0255 grams, 0.12 mmol), 5-chloro-1-propylindoline-2,3-dione, (0.015 grams, 0.067 mmol). This was taken up in 0.2 mL of methanol (purchased from Fisher Scientific). Dimethylamine (2.5 μL 40% in water purchased from Fisher Scientific) was then added and the solution heated in a Biotage initiator microwave for ten minutes at 80° C. Once complete, the reaction was concentrated using a Buchi rotoevaporator and purified using a Teledyne ISCO with silica gel (hexane, ethyl acetate gradient). Yield, 40%. 1H-NMR δ 8.06 (dd, 1H), 7.89 (t, 1H), 7.69 (dd, 1H), 7.35 (d, 1H), 7.29 (dd, 1H), 6.80 (d, 1H), 6.02 (s, 1H), 3.88 (d, 1H), 3.62 (m, 3H), 3.25 (s, 1H), 1.71 (m, 2H), (0.97 (t, 3H). calculated mass for C20H17ClN2O3, 368.09. Observed, 369.0 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09079853B2 |
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| Source dataset | uspto-grants-2015_07 |
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| ORD ID | ord-a151760c388a4bef9e4aa55bddcf01b5 |
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| Source note | uspto-grants-2015_07 |
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