2-Amino-2-methyl-1-propanol → HCID 62342457, compound
Reaction equation
[Cl:1][C:2]1[N:7]=[C:6](Cl)[CH:5]=[CH:4][N:3]=1.[NH2:9][C:10]([CH3:14])([CH3:13])[CH2:11][OH:12]>>[Cl:1][C:2]1[N:7]=[C:6]([NH:9][C:10]([CH3:14])([CH3:13])[CH2:11][OH:12])[CH:5]=[CH:4][N:3]=1Participants
3
Procedure
Prepared in analogy to example 98a), using 2,4-dichloro-pyrimidine and 2-amino-2-methylpropan-1-ol. The title compound was isolated as a yellowish solid in a yield of 19%. MS ISP (m/e): 200.3 (100) [(M+H)+]. 1H NMR (DMSO-D6, 300 MHz): δ (ppm)=7.84 (d, 1H), 7.49 (s, 1H), 6.50 (d, 1H), 4.85 (s, 1H), 3.53 (d, 2H), 1.29 (s, 6H).
Workup
- customPrepared in analogy to example 98a),
Sources & evidence
- ORD record
- ord-7f04572b2ae94744a1724b71e10e249e
- Source dataset
- uspto-grants-2015_02
- Patent number
- US08962834B2
Reaction notes
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