HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 870542Generated: October 29, 2026
Dimethylacetamide → HCID 58072102, compound
https://huagongshe.com/reaction/870542
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylacetamide | HCID 31374 | — |
| Reactant | HCID 51606335 | HCID 51606335 | — |
| Reactant | HCID 58072087 | HCID 58072087 | — |
| Product | HCID 58072102 | HCID 58072102 | — |
Reaction Steps
91 mg (R)-4-Hydroxymethyl-pyrrolidine-2-one (2.2) was placed in 1 mL of dimethylacetamide at ambient temperature under nitrogen. The reaction was stirred for 10 min before 210 mg 5-chloro-7-[3-methoxy-4-(tetrahydro-pyran-4-yloxy)-phenyl]-[1,6]naphthyridine (6.36) as a solution in 1.5 mL dimethylacetamide was introduced. The reaction was stirred overnight at ambient temperature and then heated to 70° C. where it was maintained for 2 h. After this time the mixture was cooled to ambient temperature and it was partitioned between water and ethyl acetate. The aqueous layer was separated and it was extracted with additional ethyl acetate (×2). The combined organic fractions were dried over sodium sulfate, filtered and the filtrate was concentrated under reduced pressure. Purification by silica gel chromatography (ethyl acetate/methanol: 100:0 to 92:8) gave the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08969568B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-6f5173e75e1f4bdd99402542bccf6f70 |
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| Source note | uspto-grants-2015_03 |
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