Trifluoroacetic acid → 3-(2-Amino-5-(thiophen-2-yl)phenyl)-1,1-dimethylurea

HRID 62698Notes

Reaction equation

HRID 62698 reaction equation
[CH3:1][N:2]([CH3:25])[C:3](=[O:24])[NH:4][C:5]1[CH:10]=[C:9]([C:11]2[S:12][CH:13]=[CH:14][CH:15]=2)[CH:8]=[CH:7][C:6]=1[NH:16]C(=O)OC(C)(C)C.C(O)(C(F)(F)F)=O>ClCCl>[NH2:16][C:6]1[CH:7]=[CH:8][C:9]([C:11]2[S:12][CH:13]=[CH:14][CH:15]=2)=[CH:10][C:5]=1[NH:4][C:3](=[O:24])[N:2]([CH3:1])[CH3:25]

Participants

4

Procedure

To a solution of tert-butyl (2-(3,3-dimethylureido)-4-(thiophen-2-yl)phenyl)carbamate (115 mg, 0.32 mmol) in dichloromethane (5 mL) was added TFA (2 mL) at 0° C. The reaction was warmed to room temperature and stirred for 1 h. The reaction was concentrated. The crude residue was diluted with ethyl acetate (30 mL) and washed with a saturated aqueous solution of sodium bicarbonate, then water (20 mL), dried over sodium sulfate, filtered and concentrated. The obtained residue was washed with hexane (2 mL) to afford 3-(2-amino-5-(thiophen-2-yl)phenyl)-1,1-dimethylurea (65 mg, 83% yield). ESI+ MS: m/z 262 ([M]+). 1H NMR (500 MHz, d6-DMSO): δ7.68 (s, 1H), 7.34 (d, J=5.0, 1H), 7.29 (d, J=2.0, 1H), 7.19 (dd, J=4.5, 2.0, 2H), 7.04 (m, 1H), 6.73 (d, J=8.5, 1H), 5.00 (s, 2H), 2.93 (s, 6H).

Workup

  1. concentrationThe reaction was concentrated
  2. additionThe crude residue was diluted with ethyl acetate (30 mL)
  3. washwashed with a saturated aqueous solution of sodium bicarbonate
  4. dry with materialwater (20 mL), dried over sodium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated
  7. washThe obtained residue was washed with hexane (2 mL)

Sources & evidence

ORD record
ord-dd9ee1f79afb47f29844c0e221c5bb12
Source dataset
uspto-grants-2016_09
Patent number
US09447030B2

Reaction notes

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