Dimethylamine → HCID 18917493, compound

HRID 1735260Notes

Reaction equation

[CH:1]1[CH:2]=[CH:3][N:4]2[CH2:10][C:9]3[CH:11]=[CH:12][CH:13]=[CH:14][C:8]=3[N:7]([C:15]([C:17]3[CH:22]=[CH:21][C:20]([NH:23][C:24]([C:26]4[C:27](Cl)=[N:28][CH:29]=[CH:30][CH:31]=4)=[O:25])=[CH:19][CH:18]=3)=[O:16])[CH2:6][C:5]=12.[CH3:33][NH:34][CH3:35]>>[CH:1]1[CH:2]=[CH:3][N:4]2[CH2:10][C:9]3[CH:11]=[CH:12][CH:13]=[CH:14][C:8]=3[N:7]([C:15]([C:17]3[CH:22]=[CH:21][C:20]([NH:23][C:24]([C:26]4[C:27]([N:34]([CH3:35])[CH3:33])=[N:28][CH:29]=[CH:30][CH:31]=4)=[O:25])=[CH:19][CH:18]=3)=[O:16])[CH2:6][C:5]=12

Participants

Reactant 2

HCID 674Dimethylamine

HCID 18917489HCID 18917489, compound

Product 1

HCID 18917493HCID 18917493, compound

Procedure

Using the conditions of Example 334 and 1 g of N-[4-(5H-pyrrolo[2, 1-c][1,4]benzodiazepin-10(11H) -ylcarbonyl)-phenyl]-2-chloropyridine-3-carboxamide and 10 ml of 40% N,N-dimethylamine gives 700 mg of the desired product:M+ =451.

Sources & evidence

ORD record: ord-54cd0f6aaafa4dc7b3d49b232b29a229
Source dataset: uspto-grants-1996_07
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US05536718

Reaction notes

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