(2-(2-Methoxyethoxy)ethoxy)acetic acid → HCID 60141748, compound
Reaction equation
[CH3:1][O:2][C:3]([N:5]1[C@@H:13]2[C@@H:8]([C@@:9]([OH:23])([C:14]#[C:15][C:16]3[CH:17]=[C:18]([CH3:22])[CH:19]=[CH:20][CH:21]=3)[CH2:10][CH2:11][CH2:12]2)[CH2:7][CH2:6]1)=[O:4].[CH3:24][O:25][CH2:26][CH2:27][O:28][CH2:29][CH2:30][O:31][CH2:32][C:33](O)=[O:34]>>[CH3:1][O:2][C:3]([N:5]1[C@H:13]2[C@H:8]([C@:9]([O:23][C:33](=[O:34])[CH2:32][O:31][CH2:30][CH2:29][O:28][CH2:27][CH2:26][O:25][CH3:24])([C:14]#[C:15][C:16]3[CH:17]=[C:18]([CH3:22])[CH:19]=[CH:20][CH:21]=3)[CH2:10][CH2:11][CH2:12]2)[CH2:7][CH2:6]1)=[O:4]Participants
3
Procedure
Synthesis in analogy to the General Method 1 starting from (3aS,4R,7aS)-4-hydroxy-4-m-tolylethynyl-octahydro-indole-1-carboxylic acid methyl ester and [2-(2-methoxy-ethoxy)-ethoxy]-acetic acid to yield (3aR,4S,7aR)-4-{2-[2-(2-methoxy-ethoxy)-ethoxy]-acetoxy}-4-m-tolylethynyl-octahydro-indole-1-carboxylic acid methyl ester. MS [M+H] 474; RT=7.747 min; HPLC Method I
Sources & evidence
- ORD record
- ord-5ef9b1eff67d41a4aa4df6f5a6b5ae75
- Source dataset
- uspto-grants-2015_06
- Patent number
- US09067881B2
Reaction notes
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