2-(Naphthalen-2-yl)oxirane → 2-[(1,4-Diformylpiperazin-2-yl)methoxy]-1-(1-naphthyl)ethanol
Reaction equation
C1C2C(=CC=CC=2)C=CC=1C1CO1.OCC1OCCN(C(C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)C1.[C:41]1([CH:51]2[CH2:53][O:52]2)[C:50]2[C:45](=[CH:46][CH:47]=[CH:48][CH:49]=2)[CH:44]=[CH:43][CH:42]=1.[CH:54]([N:56]1[CH2:61][CH2:60][N:59]([CH:62]=[O:63])[CH2:58][CH:57]1[CH2:64][OH:65])=[O:55]>>[CH:54]([N:56]1[CH2:61][CH2:60][N:59]([CH:62]=[O:63])[CH2:58][CH:57]1[CH2:64][O:65][CH2:53][CH:51]([C:41]1[C:50]2[C:45](=[CH:46][CH:47]=[CH:48][CH:49]=2)[CH:44]=[CH:43][CH:42]=1)[OH:52])=[O:55]Participants
5
Procedure
The same procedure as in (1) of Production Example 16 was repeated, except that the 2-(2-naphthyl)oxirane and the 2-hydroxymethyl-4-tritylmorpholine were replaced by 2-(1-naphthyl)oxirane and 1,4-diformyl-2-piperazinyl methanol, respectively, to obtain oily 2-[(1,4-diformylpiperazin-2-yl)methoxy]-1-(1-naphthyl)ethanol (compound No. 270).
Sources & evidence
- ORD record
- ord-e81ff4443ad54751baa7c16e64a24f6f
- Source dataset
- uspto-grants-1998_02
- Patent number
- US05719150
Reaction notes
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