Hydrochloric Acid → HCID 86675874, compound
Reaction equation
CC1(C)C2CC[C@@]31[C@H](C2)N([C:12](=[O:23])[C@H:13]([CH3:22])[C@H:14]([O:19][CH2:20][CH3:21])[CH2:15][CH2:16][CH:17]=[CH2:18])S(=O)(=O)C3.[OH-:27].[Li+].Cl>O1CCCC1>[CH2:20]([O:19][C@H:14]([CH2:15][CH2:16][CH:17]=[CH2:18])[C@@H:13]([CH3:22])[C:12]([OH:23])=[O:27])[CH3:21]Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of (2R,3R)-1-((1R,5S)-10,10-dimethyl-3,3-dioxo-3lambda*6*-thia-4-aza-tricyclo[5.2.1.0*1,5*]dec-4-yl)-3-ethoxy-2-methyl-hept-6-en-1-one (245 mg, 0.64 mmol) in tetrahydrofuran (12 mL) was added a lithium hydroxide solution (2 M aqueous, 5 mL). The mixture was heated to reflux for 16 hours then cooled to room temperature and acidified to pH 1 with 2 M hydrochloric acid (15 mL). The aqueous layer was extracted with ethyl acetate. The extract was dried over anhydrous sodium sulfate, filtered and evaporated to give a colourless gum, which was purified by silica gel chromatography using iso-hexanes/ether 1:1 to give the title compound (78 mg, 65%) as a colourless gum. 1H NMR (300 MHz, CDCl3) δ 1.17 (d, J=7.1 Hz, 3H), 1.20 (t, J=7.5 Hz, 3H), 1.55-1.65 (m, 2H), 2.05-2.30 (m, 2H), 2.72-2.83 (m, 1H), 3.52-3.62 (m, 3H), 4.95-5.10 (m, 2H), 5.75-5.90 (m, 1H).
Workup
- temperatureThe mixture was heated
- temperatureto reflux for 16 hours
- extractionThe aqueous layer was extracted with ethyl acetate
- dry with materialThe extract was dried over anhydrous sodium sulfate
- filtrationfiltered
- customevaporated
- customto give a colourless gum, which
- customwas purified by silica gel chromatography
Sources & evidence
- ORD record
- ord-fb27a561eb614af895811dbdfe3d593c
- Source dataset
- uspto-grants-2013_08
- Patent number
- US08513184B2
Reaction notes
Loading…