Trifluoroacetic acid → 3-(2-Amino-5-(thiophen-2-yl)phenyl)-1,1-dimethylurea
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
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
- concentrationThe reaction was concentrated
- additionThe crude residue was diluted with ethyl acetate (30 mL)
- washwashed with a saturated aqueous solution of sodium bicarbonate
- dry with materialwater (20 mL), dried over sodium sulfate
- filtrationfiltered
- concentrationconcentrated
- 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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