Triethylamine → 2-[(1S)-6-(aminocarbonyl)-3,4-dihydro-1H-2-benzopyran-1-yl]ethyl methanesulfonate
Reaction equation
[OH:1][CH2:2][CH2:3][C@H:4]1[C:9]2[CH:10]=[CH:11][C:12]([C:14]([NH2:16])=[O:15])=[CH:13][C:8]=2[CH2:7][CH2:6][O:5]1.C(N(CC)CC)C.[CH3:24][S:25](Cl)(=[O:27])=[O:26]>O1CCCC1.CN(C)C=O>[CH3:24][S:25]([O:1][CH2:2][CH2:3][C@H:4]1[C:9]2[CH:10]=[CH:11][C:12]([C:14]([NH2:16])=[O:15])=[CH:13][C:8]=2[CH2:7][CH2:6][O:5]1)(=[O:27])=[O:26]Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 2
Procedure
(1S)-1-(2-Hydroxyethyl)-3,4-dihydro-1H-2-benzopyran-6-carboxamide (5 g, 22.6 mmol) was dissolved in a mixture of dry tetrahydrofuran (375 mL) and dry dimethylformamide (15 mL) with the aid of gentle heating. Triethylamine (4.6 g, 45.5 mmol) was added, followed by methanesulfonyl chloride (2.72 g, 23.8 mmol). The mixture was stirred under nitrogen at room temperature for 1 day. The reaction mixture was quenched with water (1000 mL) and the product extracted into ethyl acetate (2×500 mL). The combined organic extracts were washed with brine (2×500 mL), dried (MgSO4), and evaporated in vacuo to give the crude product as a white solid (6.5 g, 97%). The solid was triturated with ether (300 mL) to give 2-[(1S)-6-(aminocarbonyl)-3,4-dihydro-1H-2-benzopyran-1-yl]ethyl methanesulfonate as a white solid.
Workup
- customThe reaction mixture was quenched with water (1000 mL)
- extractionthe product extracted into ethyl acetate (2×500 mL)
- washThe combined organic extracts were washed with brine (2×500 mL)
- dry with materialdried (MgSO4)
- customevaporated in vacuo
- customto give the crude product as a white solid (6.5 g, 97%)
- customThe solid was triturated with ether (300 mL)
Sources & evidence
- ORD record
- ord-e68cbc9196994e699cf1176440a53b37
- Source dataset
- uspto-grants-2008_02
- Patent number
- US07335660B2
Reaction notes
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