Isopropyl iodide → HCID 11654214, compound
Reaction equation
[NH2:1][CH2:2][C:3]1[CH:8]=[CH:7][C:6]([OH:9])=[CH:5][C:4]=1[O:10][CH3:11].I[CH:13]([CH3:15])[CH3:14].[CH3:16][C:17]1([CH3:30])[C@@H:19]2[CH2:20][C:21]3[C:25]([C@H:18]12)=[C:24]([CH3:26])[S:23][C:22]=3[C:27]([OH:29])=O>>[CH3:11][O:10][C:4]1[CH:5]=[C:6]([O:9][CH:13]([CH3:15])[CH3:14])[CH:7]=[CH:8][C:3]=1[CH2:2][NH:1][C:27]([C:22]1[S:23][C:24]([CH3:26])=[C:25]2[C:21]=1[CH2:20][C@H:19]1[C:17]([CH3:16])([CH3:30])[C@H:18]12)=[O:29]Participants
4
Procedure
(1aS,5aR)-1,1,2-Trimethyl-1,1a,5,5a-tetrahydro-3-thia-cyclopropa[a]pentalene-4-carboxylic acid 2-methoxy-4-isopropoxy-benzylamide is prepared starting from 4-aminomethyl-3-methoxy-phenol, 2-iodopropane and (1aS,5aR)-1,1,2-trimethyl-1,1a,5,5a-tetrahydro-3-thia-cyclopropa[a]pentalene-4-carboxylic acid in analogy to the procedures given in Example 36. LC-MS: tR=1.12 min, [M+1]+=400.17.
Sources & evidence
- ORD record
- ord-66b35cfbefa14c829a5b4e29c953730c
- Source dataset
- uspto-grants-2010_07
- Patent number
- US07750040B2
Reaction notes
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