Sodium Carbonate → HCID 89689588, compound

HRID 877539Notes

Reaction equation

HRID 877539 reaction equation
Cl[C:2]1[CH:9]=[C:8]([NH:10][CH:11]([CH3:13])[CH3:12])[C:5]([C:6]#[N:7])=[CH:4][N:3]=1.[NH2:14][C:15]1[CH:23]=[CH:22][C:18]2[N:19]=[CH:20][S:21][C:17]=2[CH:16]=1.CC1(C)C2C(=C(P(C3C=CC=CC=3)C3C=CC=CC=3)C=CC=2)OC2C(P(C3C=CC=CC=3)C3C=CC=CC=3)=CC=CC1=2.C([O-])([O-])=O.[Na+].[Na+]>O1CCOCC1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.[Pd].[Pd].O>[S:21]1[C:17]2[CH:16]=[C:15]([NH:14][C:2]3[CH:9]=[C:8]([NH:10][CH:11]([CH3:13])[CH3:12])[C:5]([C:6]#[N:7])=[CH:4][N:3]=3)[CH:23]=[CH:22][C:18]=2[N:19]=[CH:20]1

Participants

8

Conditions

Temperature
115 °C

Procedure

To a solution of 6-chloro-4-(isopropylamino)nicotinonitrile (18) (1 g, 5.1 mmol) in dioxane (40 mL): H2O (4 mL), 6-amino benzothiazole (5.1 mmol, 1 equiv.), xanthphos (2.0 mmol, 0.4 equiv.) and Na2CO3 (20.5 mmol, 4 equiv.) were added and degassed for 10 min. To the reaction mixture Pd2(dba)3 (2.0 mmol, 0.4 equiv.) was added and degassed again for 10 min. It was then heated at 115° C. for overnight. The reaction mixture was cooled and filtered through small pad of celite. The filtrate obtained was concentrated and the crude material was purified by column chromatography through silica gel and MeOH: CHCl3 as eluent to afford 6-(benzo[d]thiazol-6-ylamino)-4-(isopropylamino)nicotinonitrile.

Workup

  1. customdegassed for 10 min
  2. customdegassed again for 10 min
  3. temperatureThe reaction mixture was cooled
  4. filtrationfiltered through small pad of celite
  5. customThe filtrate obtained
  6. concentrationwas concentrated
  7. customthe crude material was purified by column chromatography through silica gel and MeOH

Sources & evidence

ORD record
ord-7b7c74e0f1914bf899dae16070a4c1e1
Source dataset
uspto-grants-2015_03
Patent number
US08987311B2

Reaction notes

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