HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1244327Generated: November 1, 2026
N-methyl-2-pyrrolidone → HCID 21919247, compound
https://huagongshe.com/reaction/1244327
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Reactant | Piperidin-4-ol | HCID 79341 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 178491999 | HCID 178491999 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Product | HCID 21919247 | HCID 21919247 | 70% |
Reaction Steps
0.05 g 5-Chloro-2-(4-methoxy-7-morpholin-4-yl-benzothiazol-2-yl)-3H-imidazo[4,5-b]pyridine (0.11 mmol), 0.034 g 4-hydroxypiperidine (0.34 mmol), 1 mg DMAP and 0.4 ml Hünigs base (2.2 mmol) were dissolved in NMP (1 ml). After stirring for 72 h at 120° C., the reaction mixture was concentrated and the residue taken up in water. A precipitation formed, which was filtered and dried in vacuo to yield 0.04 g 1-[3-methoxymethyl-2-(4-methoxy-7-morpholin-4-yl-benzothiazol-2-yl)-3H-imidazo[4,5-b]pyridin-5-yl]-piperidin-4-ol (70%) as a light brown solid; M.p.: 120–130° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07122545B2 |
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| Source dataset | uspto-grants-2006_10 |
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| ORD ID | ord-23ac63f6ae5849f792a206574363a4c4 |
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| Source note | uspto-grants-2006_10 |
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