2-Aminopyridine → HCID 20622841, compound

HRID 1532845Notes

Reaction equation

HRID 1532845 reaction equation
[CH3:1][O:2][C:3](=[O:28])[C@H:4]([CH2:24][CH2:25][S:26][CH3:27])[NH:5][C:6](=[O:23])[C:7]1[CH:12]=[CH:11][C:10]([CH2:13][C:14](O)=[O:15])=[CH:9][C:8]=1[C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1.ON1C(=O)C2C=CC=CC=2N=N1.[NH2:41][C:42]1[CH:47]=[CH:46][CH:45]=[CH:44][N:43]=1.Cl.CN(C)CCCN=C=NCC>CN(C)C=O.C(OCC)(=O)C>[CH3:1][O:2][C:3](=[O:28])[C@H:4]([CH2:24][CH2:25][S:26][CH3:27])[NH:5][C:6](=[O:23])[C:7]1[CH:12]=[CH:11][C:10]([CH2:13][C:14]([NH:41][C:42]2[CH:47]=[CH:46][CH:45]=[CH:44][N:43]=2)=[O:15])=[CH:9][C:8]=1[C:17]1[CH:18]=[CH:19][CH:20]=[CH:21][CH:22]=1

Participants

7

Reactant 4

HCID 104392-AminopyridineHCID 730263-hydroxy-1,2,3-benzotriazin-4(3H)-oneHCID 27239391,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 20622826HCID 20622826, compound

Product 1

HCID 20622841HCID 20622841, compound

Reagents, catalysts & solvents 2

HCID 6228DimethylformamideSolventHCID 8857Ethyl AcetateSolvent

Procedure

To a solution of the resultant acid from Example 62B (1.0 equivalent) in dimethylformamide (DMF) is added 3-hydroxy-1,2,3-benzotriazin-4(3H)-one (1.5 equivalents) followed by 2-aminopyridine (1.0 equivalent) and 1-(3-dimehtylaminopropyl)-3-ethylcarbodiimide hydrochloride (1.5 equivalents). When judged complete by TLC analysis, the reaction is taken up in ethyl acetate which is washed with 1N HCl and saturated brine, and then is dried and evaporated. The crude reaction mixture is purified by column chromatography to afford the title product.

Workup

  1. washis washed with 1N HCl and saturated brine
  2. customis dried
  3. customevaporated
  4. customThe crude reaction mixture
  5. customis purified by column chromatography

Sources & evidence

ORD record
ord-b6c29b2077be481bb988d8f13f7157bf
Source dataset
uspto-grants-2001_03
Patent number
US06204293B1

Reaction notes

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