N,N-Dimethyl-1,3-propanediamine → HCID 11541064, compound
Reaction equation
[CH3:1][C:2]([O:4][C@H:5]1[C:14]2[C@@:15]3([CH3:30])[C@@H:26]([CH2:27][O:28][CH3:29])[O:25][C:23](=[O:24])[C:17]4=[CH:18][O:19][C:20]([C:21](=[O:22])[C:13]=2[C@@H:8]2[CH2:9][CH2:10][C@H:11]([OH:12])[C@@:7]2([CH3:31])[CH2:6]1)=[C:16]34)=[O:3].[CH3:32][N:33]([CH3:38])[CH2:34][CH2:35][CH2:36][NH2:37]>C(Cl)Cl>[C:2]([O:4][C@H:5]1[C:14]2[C@:15]3([CH3:30])[C:16](/[C:17](=[CH:18]/[NH:37][CH2:36][CH2:35][CH2:34][N:33]([CH3:38])[CH3:32])/[C:23](=[O:24])[O:25][C@@H:26]3[CH2:27][O:28][CH3:29])=[C:20]([OH:19])[C:21](=[O:22])[C:13]=2[CH:8]2[C@@:7]([CH3:31])([C@@H:11]([OH:12])[CH2:10][CH2:9]2)[CH2:6]1)(=[O:3])[CH3:1]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of 100 mg (0.23 mmol) 17-hydroxywortmannin in 2 mL CH2Cl2 is added 58 μL (0.46 mmol) N,N-dimethyl-1,3-propanediamine. The reaction mixture is stirred at room temperature overnight. CH2Cl2 is removed in vacuo. The residue is triturated with Et2O to give 74 mg (60%) product as an orange powder. MS (ESI) m/z 533 (M+1).
Workup
- customCH2Cl2 is removed in vacuo
- customThe residue is triturated with Et2O
Sources & evidence
- ORD record
- ord-6c257cb0ec3a4530bf5b740c4c585308
- Source dataset
- uspto-grants-2010_02
- Patent number
- US07666901B2
Reaction notes
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