HCID 131719573, compound → HCID 131719572, compound
Reaction equation
[CH:1]([C@@H:4]1[CH2:8][C@@H:7]([C@@H:9]([N:36]=[N+:37]=[N-:38])[CH2:10][C@@H:11]([CH:33]([CH3:35])[CH3:34])[CH:12]([O:27][C:28](=[O:32])[CH:29]([CH3:31])[CH3:30])[C:13]2[CH:18]=[CH:17][C:16]([O:19][CH3:20])=[C:15]([CH2:21][CH2:22][O:23][CH2:24][O:25][CH3:26])[CH:14]=2)[O:6][C:5]1=[O:39])([CH3:3])[CH3:2]>C(N)CCC>[CH2:9]([NH:36][C:5](=[O:39])[C@H:4]([CH:1]([CH3:2])[CH3:3])[CH2:8][C@H:7]([OH:6])[C@@H:9]([N:36]=[N+:37]=[N-:38])[CH2:10][C@@H:11]([CH:33]([CH3:34])[CH3:35])[CH:12]([O:27][C:28](=[O:32])[CH:29]([CH3:30])[CH3:31])[C:13]1[CH:18]=[CH:17][C:16]([O:19][CH3:20])=[C:15]([CH2:21][CH2:22][O:23][CH2:24][O:25][CH3:26])[CH:14]=1)[CH2:7][CH2:8][CH3:4]Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of 170 mg of 3(S)-isopropyl-5(S)-{1(S)-azido-3(S)-isopropyl-4(R,S)-isobutyryloxy-4-[4-methoxy-3-(2-methoxymethoxyethyl)-phenyl]-butyl}-tetrahydrofuran-2-one in 1.4 ml of butylamine is stirred for 16 hours at room temperature and is then concentrated by evaporation. Purification of the residue by means of FC (hexane/ethyl acetate=7:3) yields the title compound: Rf (hexane/ethyl acetate=7:3)=0.25; HPLC Rt =20.38 and 20.8 minutes (diastereoisomeric mixture).
Workup
- concentrationis then concentrated by evaporation
- customPurification of the residue by means of FC (hexane/ethyl acetate=7:3)
Sources & evidence
- ORD record
- ord-59a2d63799ce4ce0a956cdad08eb308f
- Source dataset
- uspto-grants-1997_08
- Patent number
- US05654445
Reaction notes
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