HCID 10756973, compound → HCID 10504973, compound

HRID 2255316Notes

Reaction equation

HRID 2255316 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].[CH2:17]([N:24]1[C:32]2[C:27](=[CH:28][C:29](/[C:33](/[CH3:39])=[C:34](\[CH3:38])/[C:35](O)=[O:36])=[CH:30][CH:31]=2)[CH:26]=[CH:25]1)[C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1>>[CH2:17]([N:24]1[C:32]2[C:27](=[CH:28][C:29](/[C:33](/[CH3:39])=[C:34](\[CH3:38])/[C:35]([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:36])=[CH:30][CH:31]=2)[CH:26]=[CH:25]1)[C:18]1[CH:19]=[CH:20][CH:21]=[CH:22][CH:23]=1

Participants

3

Reactant 2

HCID 10756973HCID 10756973, compoundHCID 11816929Ethyl 4-(2-aminophenoxy)butanoate

Product 1

HCID 10504973HCID 10504973, compound

Procedure

0.84 g of compound 29 was obtained in a similar manner to those described in the Examples 1 and 2 using 1.13 g of ethyl 4-(2-aminophenoxy)butyrate and 0.78 g of 3-(1-benzylindol-5-yl)-2-methylisocrotonic acid obtained according to the procedures described in the Reference Examples 1-4.

Workup

  1. customobtained

Sources & evidence

ORD record
ord-2771f5303d244effbf5fdb5bbe55ad24
Source dataset
uspto-grants-1993_08
Patent number
US05239083

Reaction notes

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