Triethylamine → HCID 178449103, compound

HRID 2053795Notes

Reaction equation

HRID 2053795 reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([CH:19]=[CH:20][C:21]=1[C:22](O)=[O:23])[C:5]([NH:7][CH2:8][C:9]1[NH:13][C:12]2[CH:14]=[CH:15][C:16]([Cl:18])=[CH:17][C:11]=2[N:10]=1)=[O:6].[CH2:25]([NH:29][CH3:30])[CH:26]([CH3:28])[CH3:27].CN(C(ON1N=NC2C=CC=CC1=2)=[N+](C)C)C.[B-](F)(F)(F)F.C(N(CC)CC)C>CS(C)=O>[Cl:1][C:2]1[CH:3]=[C:4]([CH:19]=[CH:20][C:21]=1[C:22]([N:29]([CH2:25][CH:26]([CH3:28])[CH3:27])[CH3:30])=[O:23])[C:5]([NH:7][CH2:8][C:9]1[NH:13][C:12]2[CH:14]=[CH:15][C:16]([Cl:18])=[CH:17][C:11]=2[N:10]=1)=[O:6]

Participants

6

Reactant 4

HCID 8471TriethylamineHCID 12249N-MethylisobutylamineHCID 2733207O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 178523088HCID 178523088, compound

Product 1

HCID 178449103HCID 178449103, compound

Reagents, catalysts & solvents 1

HCID 679Dimethyl SulfoxideSolvent

Procedure

Prepared analogously to Example 1d from 3-chloro-N-(5-chloro-1H-benzimidazol-2-ylmethyl)-4-carboxybenzamide, N-isobutylmethylamine, TBTU, and triethylamine in DMSO at ambient temperature.

Sources & evidence

ORD record
ord-e08a1b968a5b45d0ad1437fcaf6ec1b3
Source dataset
uspto-grants-2008_02
Patent number
US07326791B2

Reaction notes

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