Thiophosgene → HCID 10287273, compound

HRID 1270348Notes

Reaction equation

HRID 1270348 reaction equation
[NH2:1][CH2:2][C:3]1[N:4]=[N:5][N:6]([C:8]2[CH:13]=[CH:12][C:11]([N:14]3[CH2:19][CH2:18][S:17](=[NH:20])[CH2:16][CH2:15]3)=[C:10]([F:21])[CH:9]=2)[CH:7]=1.[C:22](=O)(O)[O-:23].[Na+].[C:27](Cl)(Cl)=[S:28]>C(Cl)(Cl)Cl.C(OCC)(=O)C>[CH3:22][O:23][C:27](=[S:28])[NH:1][CH2:2][C:3]1[N:4]=[N:5][N:6]([C:8]2[CH:13]=[CH:12][C:11]([N:14]3[CH2:15][CH2:16][S:17](=[NH:20])[CH2:18][CH2:19]3)=[C:10]([F:21])[CH:9]=2)[CH:7]=1

Participants

6

Procedure

To an ice-cooled solution of the 4-[4-(4-aminomethyl-[1,2,3]triazol-1-yl)-2-fluoro-phenyl]-1-imino-1lambda*4*-thiomorpholine (100 mg, 0.3 mmol), obtained in Example 32 in CHCl3 (10 ml) was added sat. sodium bicarbonate solution followed by thiophosgene (36 μl, 0.33 mmol). The reaction mixture was stirred at room temperature for 0.5 h and then diluted with ethyl acetate (30 ml). The organic portion was washed with water followed by brine and dried over sodium sulfate. Evaporation of volatiles left a residue, which was refluxed with methanol (20 ml) for 20 h. Removal of volatiles and purification of the resulting residue by silica gel column chromatography (CHCl3/MeOH, 1:4) yielded the title compound as white solid (70 mg, 71%). Mp. 198° C.

Workup

  1. washThe organic portion was washed with water
  2. dry with materialdried over sodium sulfate
  3. customEvaporation of volatiles
  4. waitleft a residue, which
  5. temperaturewas refluxed with methanol (20 ml) for 20 h
  6. customRemoval of volatiles and purification of the resulting residue by silica gel column chromatography (CHCl3/MeOH, 1:4)

Sources & evidence

ORD record
ord-c7029e43f1dc42409dc394e0d38451ab
Source dataset
uspto-grants-2007_04
Patent number
US07202254B2

Reaction notes

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