HCID 19085843, compound → HCID 54208012, compound
Reaction equation
[NH:1]1[CH2:6][CH2:5][C:4]2([N:11]=[CH:10][C:9]3[CH:12]=[CH:13][CH:14]=[CH:15][C:8]=3[O:7]2)[CH2:3][CH2:2]1.BrCCCC[C:21]12[CH:31]=[CH:30][CH:29]=[CH:28][CH:22]1[C:23]([NH:25][C:26]2=[O:27])=[O:24]>>[N:1]1([CH2:2][CH2:3][CH2:4][CH2:5][C:28]2[CH:29]=[CH:30][CH:31]=[C:21]3[C:26]([NH:25][C:23](=[O:24])[C:22]=23)=[O:27])[CH2:2][CH2:3][C:4]2([N:11]=[CH:10][C:9]3[CH:12]=[CH:13][CH:14]=[CH:15][C:8]=3[O:7]2)[CH2:5][CH2:6]1Participants
3
Procedure
From spiro[2H- 1,3-benzoxazine-2,4'-piperidine] and 2-(4-bromobutyl)-phthalimide using the procedure described for Example 15, Step 5 there was obtained a white solid: mp 165°-7° C.
Workup
- customwas obtained a white solid
Sources & evidence
- ORD record
- ord-a6dc7cb17ee94f179da698c08a6adfd0
- Source dataset
- uspto-grants-1998_06
- Patent number
- US05760054
Reaction notes
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