Diisopropylethylamine → HCID 59278419, compound

HRID 1361263Notes

Reaction equation

HRID 1361263 reaction equation
[F:1][C:2]1[CH:7]=[CH:6][C:5]([N:8]2[C:12]3[CH:13]=[N:14][CH:15]=[C:16]([C:17]([OH:19])=O)[C:11]=3[CH:10]=[N:9]2)=[CH:4][CH:3]=1.CCN(C(C)C)C(C)C.CN(C(ON1N=NC2C=CC=NC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.Cl.[CH3:54][S:55]([C:58]1[CH:63]=[C:62]([C@@H:64]([NH2:66])[CH3:65])[CH:61]=[CH:60][N:59]=1)(=[O:57])=[O:56].C(=O)(O)[O-].[Na+]>CN(C=O)C.O>[CH3:54][S:55]([C:58]1[CH:63]=[C:62]([C@@H:64]([NH:66][C:17]([C:16]2[C:11]3[CH:10]=[N:9][N:8]([C:5]4[CH:4]=[CH:3][C:2]([F:1])=[CH:7][CH:6]=4)[C:12]=3[CH:13]=[N:14][CH:15]=2)=[O:19])[CH3:65])[CH:61]=[CH:60][N:59]=1)(=[O:57])=[O:56]

Participants

8

Reactant 5

HCID 81531Diisopropylethylamine2×HCID 516892Sodium BicarbonateHCID 9886157Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 592781371-(4-Fluorophenyl)-1H-pyrazolo[3,4-c]pyridine-4-carboxylic acidHCID 66727499HCID 66727499, compound

Product 1

HCID 59278419HCID 59278419, compound

Reagents, catalysts & solvents 2

HCID 962WaterSolventHCID 6228DimethylformamideSolvent2×

Procedure

To a suspension of 1-(4-fluorophenyl)-1H-pyrazolo[3,4-c]pyridine-4-carboxylic acid (17.74 g, 68.98 mmol) in DMF (200 mL) was added DIPEA (30 mL, 170 mmol) followed by HATU (27.37 g, 71.98 mmol). After 5 minutes, a light brown precipitate formed and additional DMF (50 mL) was added to aid stirring. After 1.5 hours, (S)-1-(2-methanesulfonyl-pyridin-4-yl)-ethylamine hydrochloride (14.20 g, 59.99 mmol) was added, followed by additional DIPEA (10 mL, 55 mmol). After 18 hours, the mixture was poured into water (1.5 L) containing sodium bicarbonate (25 g). The solid was collected by filtration and washed with aqueous sodium carbonate (1 L), water (1 L) and dried by pulling vacuum through the filter cake. The crude product was passed through a pad of silica gel eluting with EtOAc in dichloromethane (1:9, then 2:8, then 5:5, then 100:0). The material from the pad was concentrated and triturated with diethylether to afford the title compound as an off-white solid.

Workup

  1. customa light brown precipitate formed
  2. waitAfter 1.5 hours
  3. waitAfter 18 hours
  4. filtrationThe solid was collected by filtration
  5. washwashed with aqueous sodium carbonate (1 L), water (1 L)
  6. customdried
  7. concentrationThe material from the pad was concentrated
  8. customtriturated with diethylether

Sources & evidence

ORD record
ord-a0e2df03ae1242f9bf71d2605d53a31b
Source dataset
uspto-grants-2011_02
Patent number
US07879873B2

Reaction notes

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