Ethanolamine → HCID 85861706, compound
Reaction equation
[C:1]([NH:4][C:5]1[S:6][C:7]([C:11]2[CH:19]=[CH:18][C:14]([C:15]([OH:17])=O)=[CH:13][CH:12]=2)=[C:8]([CH3:10])[N:9]=1)(=[O:3])[CH3:2].CN(C(ON1N=NC2C=CC=NC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.CCN(C(C)C)C(C)C.[CH2:53]([CH2:55][NH2:56])[OH:54]>CN(C=O)C>[C:1]([NH:4][C:5]1[S:6][C:7]([C:11]2[CH:12]=[CH:13][C:14]([C:15]([NH:56][CH2:55][CH2:53][OH:54])=[O:17])=[CH:18][CH:19]=2)=[C:8]([CH3:10])[N:9]=1)(=[O:3])[CH3:2]Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
To 4-(2-acetylamino-4-methyl-thiazol-5-yl)-benzoic acid (Example 74b) (0.1 g, 0.36 mmol) in DMF (1 ml) is added HATU (0.14 g, 0.36 mmol) followed by DIPEA (0.07 ml, 0.36 mmol) and ethanolamine (0.022 ml, 0.36 mmol). After 5 hours, the reaction mixture is filtered and the precipitated product is washed with ethanol and dried under vacuum to give the titled compound.
Workup
- filtrationthe reaction mixture is filtered
- washthe precipitated product is washed with ethanol
- customdried under vacuum
Sources & evidence
- ORD record
- ord-4457dcabbef54dddb645d77bf18691c2
- Source dataset
- uspto-grants-2010_03
- Patent number
- US07687637B2
Reaction notes
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