HCID 10044129, compound → HCID 11757015, compound

HRID 2255329Notes

Reaction equation

HRID 2255329 reaction equation
C([CH:3]([CH2:7][CH2:8][O:9][C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][C:11]=1[NH2:16])[C:4]([OH:6])=[O:5])C.[CH2:17]([CH:22]([N:29]1[C:37]2[C:32](=[CH:33][C:34](/[C:38](/[CH3:43])=[CH:39]/[C:40](O)=[O:41])=[CH:35][CH:36]=2)[CH:31]=[CH:30]1)[C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1)[CH2:18][CH2:19][CH2:20][CH3:21]>>[CH2:17]([CH:22]([N:29]1[C:37]2[C:32](=[CH:33][C:34](/[C:38](/[CH3:43])=[CH:39]/[C:40]([NH:16][C:11]3[CH:12]=[CH:13][CH:14]=[CH:15][C:10]=3[O:9][CH2:8][CH2:7][CH2:3][C:4]([OH:6])=[O:5])=[O:41])=[CH:35][CH:36]=2)[CH:31]=[CH:30]1)[C:23]1[CH:24]=[CH:25][CH:26]=[CH:27][CH:28]=1)[CH2:18][CH2:19][CH2:20][CH3:21]

Participants

3

Reactant 2

HCID 10044129HCID 10044129, compoundHCID 19742046HCID 19742046, compound

Product 1

HCID 11757015HCID 11757015, compound

Procedure

1.01 g of compound 43 was obtained in a similar manner to those described in the Examples 1 and 2 using 1.54 g of ethyl 4-(2-aminophenoxy)butyric acid and 1.30 g of 3-[1-(α-pentylbenzyl)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-f7d7db2c5518446dbf6285f3baa49a6c
Source dataset
uspto-grants-1993_08
Patent number
US05239083

Reaction notes

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