HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 925604Generated: October 28, 2026
Diisopropylethylamine → {(2S)-1-[3-(1-Benzofuran-2-yl)imidazo[1,2-b]pyridazin-6-yl]pyrrolidin-2-yl}methanol
https://huagongshe.com/reaction/925604
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | L-Prolinol | HCID 640091 | — |
| Reactant | HCID 71491928 | HCID 71491928 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | {(2S)-1-[3-(1-Benzofuran-2-yl)imidazo[1,2-b]pyridazin-6-yl]pyrrolidin-2-yl}methanol | HCID 71144743 | — |
Reaction Steps
To a mixture of 40.5 mg (0.15 mmol) 3-(1-benzofur-2-yl)-6-chloroimidazo[1,2-b]pyridazine and 25 mg (0.195 mmol) diisopropylethylamine in 1 mL of 1-butanol were added 21 mg (0.22 mmol) (2S)-pyrrolidin-2-ylmethanol in 0.3 mL NMP. The mixture is stirred at 120° C. for 8 h. 16 mg (0.16 mmol) (2S)-pyrrolidin-2-ylmethanol in 0.2 mL NMP were added and shaking at 120° C. was continued for 8 h. Again, 16 mg (0.16 mmol) (2S)-pyrrolidin-2-ylmethanol in 0.2 mL NMP were added and shaking at 120° C. was continued for 8 h.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09284319B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-8c6a72f0505a4930ad398d31e1041c49 |
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| Source note | uspto-grants-2016_03 |
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