Diisopropylethylamine → HCID 59605655, compound
Reaction equation
[Cl:1][C:2]1[N:3]=[C:4]([N:15]2[CH2:20][CH2:19][O:18][CH2:17][CH2:16]2)[C:5]2[N:10]=[C:9]([CH2:11][C:12]([OH:14])=O)[S:8][C:6]=2[N:7]=1.[CH3:21][C:22]([N:26]1[CH2:31][CH2:30][NH:29][CH2:28][CH2:27]1)([CH3:25])[CH2:23][OH:24].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>CN(C=O)C>[Cl:1][C:2]1[N:3]=[C:4]([N:15]2[CH2:20][CH2:19][O:18][CH2:17][CH2:16]2)[C:5]2[N:10]=[C:9]([CH2:11][C:12]([N:29]3[CH2:30][CH2:31][N:26]([C:22]([CH3:25])([CH3:21])[CH2:23][OH:24])[CH2:27][CH2:28]3)=[O:14])[S:8][C:6]=2[N:7]=1Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of (5-chloro-7-morpholin-4-ylthiazolo[5,4-d]pyrimidin-2-yl)acetic acid (80 mg, 0.25 mmol), 2-methyl-2-piperazin-1-ylpropan-1-ol (48 mg, 0.31 mmol), HATU (116 mg, 0.31 mmol) and DIPEA (133 μL, 0.76 mmol) in DMF (3 mL) was stirred at r.t. for 65 h then loaded onto an Isolute® SCX-2 cartridge which was washed with MeOH and the product eluted with 2M NH3/MeOH/DCM. The resulting residue was purified by column chromatography (Si—PCC, MeOH:DCM, 0-10%) affording the title compound as an orange solid (65 mg, 56%)._LCMS (method H): RT 2.02 min [M+H]+ 455.3
Workup
- washwas washed with MeOH
- washthe product eluted with 2M NH3/MeOH/DCM
- customThe resulting residue was purified by column chromatography (Si—PCC, MeOH:DCM, 0-10%)
Sources & evidence
- ORD record
- ord-2e764d9d42d6495b92adbd8c48f17f08
- Source dataset
- uspto-grants-2012_05
- Patent number
- US08173650B2
Reaction notes
Loading…