HCID 178450729, compound → HCID 178450732, compound

HRID 1824465Notes

Reaction equation

HRID 1824465 reaction equation
[NH2:1][C@H:2]1[CH2:7][CH2:6][C@H:5]([NH2:8])[CH2:4][CH2:3]1.Cl[C:10]1[N:18]=[C:17]2[C:13]([N:14]=[CH:15][NH:16]2)=[C:12]([NH:19][C:20]2[CH:32]=[CH:31][C:23]([C:24]([O:26][CH2:27][CH2:28][CH2:29][CH3:30])=[O:25])=[CH:22][CH:21]=2)[N:11]=1>>[NH2:1][C@H:2]1[CH2:7][CH2:6][C@H:5]([NH:8][C:10]2[N:18]=[C:17]3[C:13]([N:14]=[CH:15][NH:16]3)=[C:12]([NH:19][C:20]3[CH:21]=[CH:22][C:23]([C:24]([O:26][CH2:27][CH2:28][CH2:29][CH3:30])=[O:25])=[CH:31][CH:32]=3)[N:11]=2)[CH2:4][CH2:3]1

Participants

3

Reactant 2

HCID 178450729HCID 178450729, compoundHCID 178511674HCID 178511674, compound

Product 1

HCID 178450732HCID 178450732, compoundYield 2.2%

Procedure

2850 mg of trans-1,4-diaminocyclohexane are heated to its melting point (70° C.) and 2190 mg of the product obtained in stage 1 above are added. 60 mg of the expected product are thus obtained.

Workup

  1. additionabove are added

Sources & evidence

ORD record
ord-7c18ecaf9b1243dd8eb1e29132b4c6c0
Source dataset
uspto-grants-2006_05
Patent number
US07041824B2

Reaction notes

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