Ammonium Chloride → 4-Benzothiazol-2-YL-N3-(2-ethylaminoethyl)-1H-pyrazole-3,5-diamine

HRID 407305Notes

Reaction equation

HRID 407305 reaction equation
[NH2:1][C:2]1[NH:6][N:5]=[C:4]([NH:7][CH2:8][CH2:9][NH:10][C:11](=O)[CH3:12])[C:3]=1[C:14]1[S:15][C:16]2[CH:22]=[CH:21][CH:20]=[CH:19][C:17]=2[N:18]=1.[H-].[Al+3].[Li+].[H-].[H-].[H-].[Cl-].[NH4+]>C1COCC1>[S:15]1[C:16]2[CH:22]=[CH:21][CH:20]=[CH:19][C:17]=2[N:18]=[C:14]1[C:3]1[C:4]([NH:7][CH2:8][CH2:9][NH:10][CH2:11][CH3:12])=[N:5][NH:6][C:2]=1[NH2:1]

Participants

5

Procedure

N-[2-(5-Amino-4-benzothiazol-2-yl-1H-pyrazol-3-ylamino)ethyl]acetamide (80 mg, 0.25 mmol) and lithium aluminum hydride (92 mg) were refluxed in anhydrous THF (10 mL) for 3 hrs. The resulting mixture was poured into a saturated ammonium chloride solution (50 mL). The aqueous phase was extracted with ethyl acetate (3×50 mL). The combined extracts were washed with brine, dried over anhydrous sodium sulfate, filtered and evaporated to yield 54 mg of crude product. The crude product was purified by flash column chromatography eluting with CH2Cl2:MeOH=5:1 with 0.5% NH3. The title compound was isolated in a yield of 36 mg (48%). MS (m/z, ES+): 303.1 (M+1, 100%).

Workup

  1. extractionThe aqueous phase was extracted with ethyl acetate (3×50 mL)
  2. washThe combined extracts were washed with brine
  3. dry with materialdried over anhydrous sodium sulfate
  4. filtrationfiltered
  5. customevaporated
  6. customto yield 54 mg of crude product
  7. customThe crude product was purified by flash column chromatography
  8. washeluting with CH2Cl2

Sources & evidence

ORD record
ord-8533f19ff4ac461485603d5332df8b7a
Source dataset
uspto-grants-2014_06
Patent number
US08754233B2

Reaction notes

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