1,2-Dichloroethane → HCID 25017920, compound
Reaction equation
[F:1][C:2]1[C:10]([O:11][C:12]2[C:21]3[C:16](=[CH:17][C:18]([O:24][CH2:25][C:26]4([C:29]([OH:31])=O)[CH2:28][CH2:27]4)=[C:19]([O:22][CH3:23])[CH:20]=3)[N:15]=[CH:14][CH:13]=2)=[CH:9][CH:8]=[C:7]2[C:3]=1[CH:4]=[C:5]([CH3:32])[NH:6]2.C[CH2:34][N:35](C(C)C)[CH:36](C)C.C(Cl)CCl.C1C=CC2N(O)N=NC=2C=1.Cl.CNC>C(Cl)Cl>[F:1][C:2]1[C:10]([O:11][C:12]2[C:21]3[C:16](=[CH:17][C:18]([O:24][CH2:25][C:26]4([C:29]([N:35]([CH3:36])[CH3:34])=[O:31])[CH2:28][CH2:27]4)=[C:19]([O:22][CH3:23])[CH:20]=3)[N:15]=[CH:14][CH:13]=2)=[CH:9][CH:8]=[C:7]2[C:3]=1[CH:4]=[C:5]([CH3:32])[NH:6]2Participants
7
Procedure
The product of Example 10 (100 mg) was mixed with DIPEA (1.5 eq), EDC (1.25 eq), HOBt (1 eq) and dimethylamine hydrochloride (3 eq) in DCM (20 ml). The reaction was stirred at RT overnight and washed with NaHCO3 solution, dried. The solution was evaporated and purified with silica gel column to give the titled product (80 mg). Mass: (M+1), 464
Workup
- washwashed with NaHCO3 solution
- customdried
- customThe solution was evaporated
- custompurified with silica gel column
Sources & evidence
- ORD record
- ord-b09d1d488dea4f619c1f1bb8c0817a9f
- Source dataset
- uspto-grants-2012_04
- Patent number
- US08148532B2
Reaction notes
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