Ethyl 4-[3-[8-(4-isobutylphenyl)undecanoyl]1-indolyl]butyrate → HCID 178444534, compound

HRID 260850Notes

Reaction equation

HRID 260850 reaction equation
[CH2:1]([C@H:6]1[CH2:11][CH2:10][C@H:9]([C:12]([C:14]2[C:22]3[C:17](=[CH:18][CH:19]=[CH:20][CH:21]=3)[N:16]([CH2:23][CH2:24][CH2:25][C:26]([O:28]CC)=[O:27])[CH:15]=2)=[O:13])[CH2:8][CH2:7]1)[CH2:2][CH2:3][CH2:4][CH3:5].C(C1C=CC(C(CCC)CCCCCCC(C2C3C(=CC=CC=3)N(CCCC(OCC)=O)C=2)=O)=CC=1)C(C)C>>[CH2:1]([C@H:6]1[CH2:11][CH2:10][C@H:9]([C:12]([C:14]2[C:22]3[C:17](=[CH:18][CH:19]=[CH:20][CH:21]=3)[N:16]([CH2:23][CH2:24][CH2:25][C:26]([OH:28])=[O:27])[CH:15]=2)=[O:13])[CH2:8][CH2:7]1)[CH2:2][CH2:3][CH2:4][CH3:5]

Participants

3

Reactant 2

HCID 22400460Ethyl 4-[3-[8-(4-isobutylphenyl)undecanoyl]1-indolyl]butyrateHCID 178444535HCID 178444535, compound

Product 1

HCID 178444534HCID 178444534, compound

Procedure

The procedure of Ex. 16 was repeated except that transethyl 4-[3-(4-pentylcyclohexylcarbonyl)-1-indolyl]butyrate obtained in Ex. 32 was used in place of ethyl 4-[3-[8-(4-isobutylphenyl) undecanoyl]-1-indolyl]butyrate to give trans-4-[3-(4-pentylcyclohexylcarbonyl)-1-indolyl]butyric acid.

Workup

  1. customobtained in Ex

Sources & evidence

ORD record
ord-19b23137bd4143ec84bc6fbde3da1b79
Source dataset
uspto-grants-1996_06
Patent number
US05530019

Reaction notes

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