Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyrrolidine | HCID 31268 | — |
| Reactant | HCID 11305377 | HCID 11305377 | — |
| Product | HCID 21919250 | HCID 21919250 | 74% |
Reaction Steps
0.1 g 5-Chloro-3-methoxymethyl-2-(4-methoxy-7-morpholin-4-yl-benzothiazol-2-yl)-3H-imidazo[4,5-b]pyridine (0.22 mmol) was dissolved in pyrrolidine (5 ml) in an autoclave and heated to 130° C. for 16 h. The residue was triturated in water whereupon a precipitate formed, which was isolated and dried in vacuo. 0.08 g 3-methoxymethyl-2-(4-methoxy-7-morpholin-4-yl-benzothiazol-2-yl)-5-pyrrolidin-4-yl-3H-imidazo[4,5-b]pyridine (74%) were obtained as a yellow 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-b09c0ad448d546f3a66f1db21ec1bfd9 |
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| Source note | uspto-grants-2006_10 |
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