Sodium Carbonate → 2-(6-Methoxypyridin-3-yl)-1,3-benzothiazol-6-amine

HRID 1851754Notes

Reaction equation

HRID 1851754 reaction equation
Br[C:2]1[S:3][C:4]2[CH:10]=[C:9]([NH2:11])[CH:8]=[CH:7][C:5]=2[N:6]=1.[CH3:12][O:13][C:14]1[CH:19]=[CH:18][C:17](B(O)O)=[CH:16][N:15]=1.C(=O)([O-])[O-].[Na+].[Na+]>C1COCC1.O.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.Cl[Pd]Cl.[Fe+2]>[CH3:12][O:13][C:14]1[N:15]=[CH:16][C:17]([C:2]2[S:3][C:4]3[CH:10]=[C:9]([NH2:11])[CH:8]=[CH:7][C:5]=3[N:6]=2)=[CH:18][CH:19]=1

Participants

6

Reactant 3

HCID 10340Sodium CarbonateHCID 2734368(6-Methoxypyridin-3-yl)boronic acidHCID 529878072-Bromobenzo[d]thiazol-6-amine

Product 1

HCID 248035652-(6-Methoxypyridin-3-yl)-1,3-benzothiazol-6-amineYield 96.3%

Reagents, catalysts & solvents 2

HCID 178418228Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)CatalystHCID 21881883Oxolane--water (1/1)Solvent

Conditions

Temperature
140 °C

Procedure

A mixture of 2-bromo-1,3-benzothiazol-6-amine (53 mg, 0.23 mmol), 2-methoxy-5-pyridineboronic acid (50 mg, 0.327 mmol), Pd(dppf)Cl2*DCM (8 mg, 0.01 mmol) and sodium carbonate (0.1 g, 1 mmol) in THF/water (9:1, 3 mL) was heated at 140° C. for 10 minutes in a microwave reactor under argon atmosphere. The mixture was filtered and washed with THF/water (9:1). After having added DCM to the filtrate, the organic layer to was washed with brine, dried (Na2SO4), filtered and concentrated. The crude product was purified by flash column chromatography (20 to 70% ethyl acetate in heptane), to yield the title compound (57 mg) as an off-white solid. 1H NMR. (CHLOROFORM-d) δ 8.68 (d, 1H) 8.16 (dd, 1 H) 7.74 (d, 1 H) 7.06 (d, 1 H) 6.70-6.81 (m, 2 H) 3.94 (s, 3 H) 3.77 (s, 2 H); MS m/z (M+H) 258.

Workup

  1. filtrationThe mixture was filtered
  2. washwashed with THF/water (9:1)
  3. additionAfter having added DCM to the filtrate
  4. washthe organic layer to was washed with brine
  5. dry with materialdried (Na2SO4)
  6. filtrationfiltered
  7. concentrationconcentrated
  8. customThe crude product was purified by flash column chromatography (20 to 70% ethyl acetate in heptane)

Sources & evidence

ORD record
ord-bf8cbdad2f194576b22b1057ff9529df
Source dataset
uspto-grants-2015_02
Patent number
US08957215B2

Reaction notes

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