HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 495447Generated: October 29, 2026
HCID 22326713, compound → HCID 22326660, compound
https://huagongshe.com/reaction/495447
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 22326713 | HCID 22326713 | — |
| Reactant | HCID 178418546 | HCID 178418546 | — |
| Product | HCID 22326660 | HCID 22326660 | 23.5% |
Reaction Steps
A mixture of 6-{1-[2-(7-Iodo-2-methyl-quinolin-5-yloxy)-ethyl]-piperidin-4-ylmethyl}-4H-benzo[1,4]oxazin-3-one (155 mg, 0.28 mmol) and copper (I) cyanide (50 mg, 0.56 mmol) in N-methylpyrrolidinione (2 mL) was stirred at 90° C. for 18 hrs. Upon cooling to room temperature the reaction mixture was partitioned between dichloromethane (5 mL) and ammonia (0.880, 5 mL). The organic layer was separated and applied directly to a 10 g pre-packed silica column eluting with 0-20% methanol in ethyl acetate to afford the title compound as a yellow oil (30 mg, 23%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06939871B2 |
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| Source dataset | uspto-grants-2005_09 |
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| ORD ID | ord-2f85803f8e6343af996fa16acdb9017c |
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| Source note | uspto-grants-2005_09 |
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