Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | 1-Chloro-N,N-2-trimethylpropenylamine | HCID 640792 | — |
| Reactant | Methyl 4-[2-(4-{[(2-amino-4,5,6,7-tetrahydro-1-benzothiophen-3-yl)carbonyl]amino}phenyl)ethyl]benzoate | HCID 68207883 | — |
| Reactant | HCID 90370043 | HCID 90370043 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 90370352 | HCID 90370352 | 97.6% |
Reaction Steps
To a mixture of 480 mg of 3-(2-{[tert-butyl(diphenyl)silyl]oxy}ethyl)benzoic acid and 10 ml of methylene chloride was added 160 mg of 1-chloro-N,N,2-trimethylpropenylamine under ice cooling, followed by stirring for 1 hour at room temperature. 10 ml of a methylene chloride solution containing 450 mg of methyl 4-[2-(4-{[(2-amino-4,5,6,7-tetrahydro-1-benzothiophen-3-yl)carbonyl]amino}phenyl)ethyl]benzoate and 0.20 mL of pyridine was added to the reaction mixture under ice cooling, followed by stirring for 1 hour under ice cooling and then for 4 days at room temperature. The reaction mixture was concentrated under reduced pressure, ethyl acetate and water were added thereto, and the organic layer was separated. The organic layer was washed with a 5% aqueous citric acid solution, a saturated aqueous sodium hydrogen carbonate solution, and saturated brine in this order and dried over anhydrous sodium sulfate, and the solvent was removed under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=1:1), thereby obtaining 830 mg of methyl 4-[2-(4-{[(2-{[3-(2-{[tert-butyl(diphenyl)silyl]oxy}ethyl)benzoyl]amino}-4,5,6,7-tetrahydro-1-benzothiophen-3-yl)carbonyl]amino}phenyl)ethyl]benzoate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09062032B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-d57270688f23474e88ce41de9831a0c9 |
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| Source note | uspto-grants-2015_06 |
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