Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 59809564 | HCID 59809564 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 59809539 | HCID 59809539 | — |
Reaction Steps
To a suspension of sodium hydride (0.1-1 g; 0.74 mmol) in DMF (5 mL) was added a solution of 4-[2-(2-bromophenoxy)-4-cyanophenylamino]-piperidine-1-carboxylic acid tert-butyl ester, 3a (0.35 g; 0.74 mmol) in DMF (3 mL). The mixture was heated to 120° C. for 90 min and allowed to cool to rt. The mixture was poured into ice-water and a precipitate formed. The solid was separated via filtration, dried to yield 4-(3-cyanophenoxazin-10-yl)-piperidine-1-carboxylic acid tert-butyl ester, 4a. MS m/z (M+Na) 413.9. The material was used as such for the next reaction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07432257B2 |
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| Source dataset | uspto-grants-2008_10 |
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| ORD ID | ord-657dbedd513e47ed938e84303ac7bbb5 |
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| Source note | uspto-grants-2008_10 |
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