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2-Amino-2-methyl-1-propanol → 1-(1-Hydroxy-2-methylpropan-2-yl)-3-[4-(trifluoromethoxy)phenyl]urea

HRID 711302
Notes
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Reaction equation

HRID 711302 reaction equation
CC1(C)CCN(C2C=CC(SC(F)(F)F)=CC=2)C(=O)N1CC1C2C(=NC=CC=2)NC=1.[NH2:31][C:32]([CH3:36])([CH3:35])[CH2:33][OH:34].[F:37][C:38]([F:50])([F:49])[O:39][C:40]1[CH:45]=[CH:44][C:43]([N:46]=[C:47]=[O:48])=[CH:42][CH:41]=1>>[OH:34][CH2:33][C:32]([NH:31][C:47]([NH:46][C:43]1[CH:44]=[CH:45][C:40]([O:39][C:38]([F:37])([F:49])[F:50])=[CH:41][CH:42]=1)=[O:48])([CH3:36])[CH3:35]
ParticipantsProcedureSources & evidenceReaction notes

Participants

4

Reactant 3

HCID 118072-Amino-2-methyl-1-propanolHCID 92298p-(Trifluoromethoxy)phenyl isocyanateHCID 722044234,4-dimethyl-3-(1H-pyrrolo[2,3-b]pyridin-3-ylmethyl)-1-{4-[(trifluoromethyl)sulfanyl]phenyl}tetrahydropyrimidin-2(1H)-one

Product 1

HCID 900141051-(1-Hydroxy-2-methylpropan-2-yl)-3-[4-(trifluoromethoxy)phenyl]urea

Procedure

1-(1-hydroxy-2-methylpropan-2-yl)-3-[4-(trifluoromethoxy)phenyl]urea was prepared similar to compound 5, but the following reagents were used: 2-amino-2-methyl-1-propanol and 4-(trifluoromethoxy)phenylisocyanate. LCMS [M+H]+=293.1.

Sources & evidence

ORD record
ord-8681fdd4225a46349b7174c2342a94ca
Source dataset
uspto-grants-2015_11
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US09181261B2

Reaction notes

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On this pageParticipantsProcedureSources & evidenceReaction notes