Isopropanol → HCID 59737255, compound
Reaction equation
[CH3:1][O:2][C:3]1[CH:28]=[CH:27][C:6]([C:7]([NH:9][C:10]2[CH:11]=[C:12]([C:19]3[CH:24]=[CH:23][C:22]([S:25][CH3:26])=[CH:21][CH:20]=3)[CH:13]=[CH:14][C:15]=2[N+:16]([O-])=O)=[O:8])=[CH:5][CH:4]=1.C([OH:32])(C)C>C(Cl)Cl>[NH2:16][C:15]1[CH:14]=[CH:13][C:12]([C:19]2[CH:24]=[CH:23][C:22]([S:25]([CH3:26])=[O:32])=[CH:21][CH:20]=2)=[CH:11][C:10]=1[NH:9][C:7](=[O:8])[C:6]1[CH:27]=[CH:28][C:3]([O:2][CH3:1])=[CH:4][CH:5]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Following the same procedure as described in Example 10, step 2 (scheme 10), but substituting compound 120 for compound 209, the title compound 210 was obtained in 57% yield [after column chromatography (5% isopropanol in DCM)].
Sources & evidence
- ORD record
- ord-c9d4159010454d04b2449b242ad101aa
- Source dataset
- uspto-grants-2013_12
- Patent number
- US08598168B2
Reaction notes
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