HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1098317Generated: November 2, 2026
Sodium Bicarbonate → 2-Fluoro-6,n,n-trimethyl-3-morpholin-4-ylbenzamide
https://huagongshe.com/reaction/1098317
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 1,1'-Difluoro-2,2'-bipyridinium Bis(tetrafluoroborate) | HCID 2733931 | — |
| Reactant | 2,N,N-Trimethyl-5-morpholin-4-ylbenzamide | HCID 23156788 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-Fluoro-6,n,n-trimethyl-3-morpholin-4-ylbenzamide | HCID 23156760 | 7.2% |
| Product | 4-fluoro-2,N,N-trimethyl-5-morpholin-4-ylbenzamide | HCID 23156865 | 5.3% |
Reaction Steps
393 mg (1.10 mmol) of N,N′-difluoro-2,2′-bipyridinium bis(tetrafluoroborate) was added to 7 ml of an acetonitrile solution containing 458 mg (1.84 mmol) of the 2, N,N-trimethyl-5-morpholin-4-ylbenzamide obtained in Step B of Example 80 under cooling on ice. The obtained mixture was stirred at 0° C. for 1 hour, then at a room temperature for 1 hour, then at 50° C. for 1 hour, then at 80° C. for 2.5 days, and then under heating to reflux for 2 hours. Thereafter, 357 mg (1.0 mmol) of N,N′-difluoro-2,2′-bipyridinium bis(tetrafluoroborate) was further added to the reaction solution, and the obtained mixture was further stirred for 20 minutes. Thereafter, a saturated sodium bicarbonate aqueous solution was added to the reaction solution, and the mixture was then extracted with ethyl acetate. The extract was dried over anhydrous sodium sulfate, and was then concentrated. The obtained residue was purified by silica gel column chromatography (ethyl acetate:hexane=1:3 to 1:1), so as to obtain 25.8 mg (5.3%) of 4-fluoro-2,N,N-trimethyl-5-morpholin-4-ylbenzamide in the form of an oily substance, and also obtain 35.1 mg (7.2%) of 2-fluoro-6,N,N-trimethyl-3-morpholin-4-ylbenzamide in the form of an oily substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08143274B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-fe6ed1284d814452a0c7f1e5510c64a0 |
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| Source note | uspto-grants-2012_03 |
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