HCID 53685115, compound → N-methyl-N-phenethyl-2-[4-benzyloxy-3-(2-carboxy-2-ethylvinyl)indol-1-yl]acetamide
Reaction equation
CN(CCC1C=CC=CC=1)[C:3](=O)[CH2:4]N1C2C(=CC(OCC3C=CC=CC=3)=CC=2)C(C=CC(OCC)=O)=C1.[CH3:38][N:39]([CH2:67][CH2:68][C:69]1[CH:74]=[CH:73][CH:72]=[CH:71][CH:70]=1)[C:40](=[O:66])[CH2:41][N:42]1[C:50]2[C:45](=[C:46]([O:51][CH2:52][C:53]3[CH:58]=[CH:57][CH:56]=[CH:55][CH:54]=3)[CH:47]=[CH:48][CH:49]=2)[C:44]([CH:59]=[CH:60][C:61]([O:63]CC)=[O:62])=[CH:43]1.CN(CCC1C=CC=CC=1)C(=O)CN1C2C(=C(OCC3C=CC=CC=3)C=CC=2)C(C=CC(O)=O)=C1>>[CH3:38][N:39]([CH2:67][CH2:68][C:69]1[CH:70]=[CH:71][CH:72]=[CH:73][CH:74]=1)[C:40](=[O:66])[CH2:41][N:42]1[C:50]2[C:45](=[C:46]([O:51][CH2:52][C:53]3[CH:54]=[CH:55][CH:56]=[CH:57][CH:58]=3)[CH:47]=[CH:48][CH:49]=2)[C:44]([CH:59]=[C:60]([C:61]([OH:63])=[O:62])[CH2:3][CH3:4])=[CH:43]1Participants
4
Reactant 3
Product 1
Procedure
When N-methyl-N-phenethyl-2-[5-benzyloxy-3-(2-carboethoxyvinyl)-indol-1-yl]acetamide in the procedure of Example 23 is replaced with N-methyl-N-phenethyl-2-[4-benzyloxy-3-(2-carboethoxyvinyl)indol-1-yl]acetamide then the product prepared is N-methyl-N-phenethyl-2-[4-benzyloxy-3-(2-carboxyvinyl)indol-1-yl]acetamide as a white powder. (m.p. 170°-174° C.)
Workup
- customthe product prepared
Sources & evidence
- ORD record
- ord-1cecf86250334ce1aee88362811ca3ad
- Source dataset
- uspto-grants-1995_11
- Patent number
- US05468898
Reaction notes
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