HCID 10767818, compound → HCID 10741141, compound

HRID 479595Notes

Reaction equation

HRID 479595 reaction equation
[CH2:1]([O:8][C:9]1[C:17]2[N:13]([C:14]([C:25](=[O:38])[C:26]3[CH:31]=[CH:30][CH:29]=[CH:28][C:27]=3C3C=CC=CC=3)=[C:15]([CH2:23][CH3:24])[C:16]=2[C:18]([O:20][CH2:21][CH3:22])=[O:19])[CH:12]=[CH:11][CH:10]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1>CCOC(C)=O.CCCCCC>[C:25]([C:14]1[N:13]2[C:17]([C:9]([O:8][CH2:1][C:2]3[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=3)=[CH:10][CH:11]=[CH:12]2)=[C:16]([C:18]([O:20][CH2:21][CH3:22])=[O:19])[C:15]=1[CH2:23][CH3:24])(=[O:38])[C:26]1[CH:27]=[CH:28][CH:29]=[CH:30][CH:31]=1

Participants

3

Reactant 1

HCID 10767818HCID 10767818, compound

Product 1

HCID 10741141HCID 10741141, compoundYield 79%

Reagents, catalysts & solvents 1

HCID 21226206Ethyl acetate hexaneSolvent

Procedure

Mp, 124-125° C. (AcOEt-hexane). 79% Yield. Ethyl (8-benzyloxy-2-ethyl-3-(o-phenylbenzoyl)indolizin-1-yl)carboxylate 26b. Mp, 110-112° C. (ether-hexane). 46.0% Yield.

Sources & evidence

ORD record
ord-0a1b14738d894d83acfb99a540680152
Source dataset
uspto-grants-2003_11
Patent number
US06645976B1

Reaction notes

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