HCID 12446101, compound → HCID 69072678, compound

HRID 2273558Notes

Reaction equation

HRID 2273558 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 12446101HCID 12446101, compoundHCID 57505785HCID 57505785, compound

Product 1

HCID 69072678HCID 69072678, compound

Procedure

By following the processes described in stages A to C of Example R13, Example R36 is prepared by dimerization of [3-(ethoxycarbonyl)phenoxy]acetic acid with 1,2-cis-cyclopropanediamine (CAS 365996-16-3). A white powder is obtained.

Workup

  1. customA white powder is obtained

Sources & evidence

ORD record
ord-687045d9260c4724b8a08b70889d08fc
Source dataset
uspto-grants-2015_09
Patent number
US09120819B2

Reaction notes

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