HCID 9993344, compound → HCID 10049336, compound

HRID 2255309Notes

Reaction equation

HRID 2255309 reaction equation
[NH2:1][C:2]1[CH:16]=[CH:15][CH:14]=[CH:13][C:3]=1[O:4][CH2:5][CH2:6][CH2:7][C:8]([O:10]CC)=[O:9].[CH3:17][CH:18]([N:22]1[C:30]2[C:25](=[CH:26][C:27](/[C:31](/[CH3:36])=[CH:32]/[C:33](O)=[O:34])=[CH:28][CH:29]=2)[CH:24]=[CH:23]1)[CH2:19][CH2:20][CH3:21]>>[CH3:17][CH:18]([N:22]1[C:30]2[C:25](=[CH:26][C:27](/[C:31](/[CH3:36])=[CH:32]/[C:33]([NH:1][C:2]3[CH:16]=[CH:15][CH:14]=[CH:13][C:3]=3[O:4][CH2:5][CH2:6][CH2:7][C:8]([OH:10])=[O:9])=[O:34])=[CH:28][CH:29]=2)[CH:24]=[CH:23]1)[CH2:19][CH2:20][CH3:21]

Participants

3

Reactant 2

HCID 9993344HCID 9993344, compoundHCID 11816929Ethyl 4-(2-aminophenoxy)butanoate

Product 1

HCID 10049336HCID 10049336, compound

Procedure

1.20 g of compound 16 was obtained in a similar manner to those described in the Examples 1 and 2 using 2.63 g of ethyl 4-(2-aminophenoxy)butyrate and 1.60 g of 3-[1-(1-methylbutyl)indol-5-yl]isocrotonic acid obtained according to the procedures described in the Reference Examples 1-4.

Workup

  1. customobtained

Sources & evidence

ORD record
ord-ac50de15463146fc814bf0feaf5d524b
Source dataset
uspto-grants-1993_08
Patent number
US05239083

Reaction notes

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