4-Methylmorpholine → HCID 16222130, compound
Reaction equation
[CH:1]1([C:7]([NH:9][C:10]2[CH:11]=[CH:12][C:13]([CH3:25])=[C:14]([C:16]3[CH:21]=[CH:20][C:19]([C:22](O)=[O:23])=[CH:18][CH:17]=3)[CH:15]=2)=[O:8])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[O:26]=[S:27]1(=[O:42])[CH2:32][CH2:31][N:30]([CH2:33][CH2:34][C:35]2[CH:40]=[CH:39][C:38]([NH2:41])=[CH:37][CH:36]=2)[CH2:29][CH2:28]1.CCN=C=NCCCN(C)C.C1C=CC2N(O)N=NC=2C=1.CN1CCOCC1>CN(C=O)C.O>[O:42]=[S:27]1(=[O:26])[CH2:28][CH2:29][N:30]([CH2:33][CH2:34][C:35]2[CH:40]=[CH:39][C:38]([NH:41][C:22]([C:19]3[CH:20]=[CH:21][C:16]([C:14]4[CH:15]=[C:10]([NH:9][C:7]([CH:1]5[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]5)=[O:8])[CH:11]=[CH:12][C:13]=4[CH3:25])=[CH:17][CH:18]=3)=[O:23])=[CH:37][CH:36]=2)[CH2:31][CH2:32]1Participants
8
Reactant 5
Product 1
Reagents, catalysts & solvents 2
Procedure
A mixture of 5′-(Cyclohexanecarbonyl-amino)-2′-methyl-biphenyl-4-carboxylic acid (40 mg), 4-[2-(1,1-dioxo-1lambda*6*-thiomorpholin-4-yl)-ethyl]-phenylamine (30 mg), EDAC (23 mg), HOBT (16 mg) and N-Methylmorpholine (26 μl) in dry DMF (1 ml) was stirred for 16 hrs. This mixture was then diluted with water (8 ml) and the tan solid produced collected and dried (45 mg).
Workup
- customthe tan solid produced
- customcollected
- customdried (45 mg)
Sources & evidence
- ORD record
- ord-bbef08403bd9416293253e1c0f15d056
- Source dataset
- uspto-grants-2011_08
- Patent number
- US08008303B2
Reaction notes
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