HCID 12446102, compound → HCID 69069273, compound

HRID 2273557Notes

Reaction equation

HRID 2273557 reaction equation
C([O:3][C:4]([C:6]1[CH:7]=[C:8]([CH:14]=[CH:15][CH:16]=1)[O:9][CH2:10][C:11]([OH:13])=O)=[O:5])C.[C@@H:17]1([NH2:21])[CH2:19][C@H:18]1[NH2:20]>>[C@@H:17]1([NH:21][C:11](=[O:13])[CH2:10][O:9][C:8]2[CH:7]=[C:6]([CH:16]=[CH:15][CH:14]=2)[C:4]([OH:3])=[O:5])[CH2:19][C@H:18]1[NH:20][C:11](=[O:13])[CH2:10][O:9][C:8]1[CH:7]=[C:6]([CH:16]=[CH:15][CH:14]=1)[C:4]([OH:5])=[O:3]

Participants

3

Reactant 2

HCID 12446102HCID 12446102, compoundHCID 57505785HCID 57505785, compound

Product 1

HCID 69069273HCID 69069273, compound

Procedure

By following the processes described in stages A to C of Example R13, Example R35 is prepared by dimerization of [3-(ethoxycarbonyl)phenoxy]acetic acid with 1,2-trans-cyclopropanediamine (CAS 758637-65-9). A white powder is obtained.

Workup

  1. customA white powder is obtained

Sources & evidence

ORD record
ord-27c4e61d908c45bc9404165bf9f79877
Source dataset
uspto-grants-2015_09
Patent number
US09120819B2

Reaction notes

Loading…