Sulfamic Acid → HCID 86592863, compound

HRID 1643229Notes

Reaction equation

HRID 1643229 reaction equation
[O:1]1[C:5]2[CH:6]=[CH:7][C:8]([CH2:10][N:11]([C:22]3[N:26]([CH2:27][CH2:28][CH2:29][CH3:30])[C:25]([C:31]4[CH:36]=[CH:35][CH:34]=[CH:33][CH:32]=4)=[N:24][C:23]=3[CH:37]=[O:38])[CH2:12][C:13]3[CH:21]=[CH:20][C:16]4[O:17][CH2:18][O:19][C:15]=4[CH:14]=3)=[CH:9][C:4]=2[O:3][CH2:2]1.S(=O)(=O)([OH:41])N.Cl([O-])=O.[Na+]>O>[O:1]1[C:5]2[CH:6]=[CH:7][C:8]([CH2:10][N:11]([C:22]3[N:26]([CH2:27][CH2:28][CH2:29][CH3:30])[C:25]([C:31]4[CH:32]=[CH:33][CH:34]=[CH:35][CH:36]=4)=[N:24][C:23]=3[C:37]([OH:41])=[O:38])[CH2:12][C:13]3[CH:21]=[CH:20][C:16]4[O:17][CH2:18][O:19][C:15]=4[CH:14]=3)=[CH:9][C:4]=2[O:3][CH2:2]1

Participants

5

Procedure

To a solution of 5-[(bis-benzo[1,3]dioxol-5-ylmethyl-amino]-1-butyl-2-phenyl-1H-imidazol-4-carbaldehyde 213 (263 mg, 0.5 mmol) in actone (10 mL) and water (5 mL) is added sulfamic acid (107 mg, 1.1 mmol) at room temperature and the mixture is stirred for 30 min. Sodium chlorite (63 mg, 0.7 mmol) is added and the mixture is stirred for additional 30 men at room temperature. Evaporation of most actone and the residure is extracted with chloroform. The organic phase is washed with water, brine and dried over sodium sulfate. The solvent is removed aid the product is dried in vacuo. Yield: 281 mg; LC-MS (MH+): 542.

Workup

  1. stirringthe mixture is stirred for additional 30 men at room temperature
  2. customEvaporation of most actone
  3. extractionthe residure is extracted with chloroform
  4. washThe organic phase is washed with water, brine
  5. dry with materialdried over sodium sulfate
  6. customThe solvent is removed aid the product
  7. customis dried in vacuo

Sources & evidence

ORD record
ord-8c21c6dc79c944bb8950026e01492728
Source dataset
uspto-grants-2012_02
Patent number
US08119665B2

Reaction notes

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