HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 426080Generated: October 31, 2026
Diisopropylethylamine → 3-Bromo-N-((2S)-2-(4-fluorophenyl)-4-{3-[4-(morpholin-4-ylcarbonyl)piperidin-1-yl]azetidin-1-yl}butyl)-N-methyl-5-(trifluoromethyl)benzamide
https://huagongshe.com/reaction/426080
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | N-[(2S)-4-{3-[4-(Azetidin-1-ylcarbonyl)piperidin-1-yl]azetidin-1-yl}-2-(4-fluorophenyl)butyl]-3-bromo-N-methyl-5-(trifluoromethyl)benzamide | HCID 23582759 | — |
| Reactant | 4-[(1-Azetidin-3-ylpiperidin-4-yl)carbonyl]morpholine | HCID 23658957 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-Bromo-N-((2S)-2-(4-fluorophenyl)-4-{3-[4-(morpholin-4-ylcarbonyl)piperidin-1-yl]azetidin-1-yl}butyl)-N-methyl-5-(trifluoromethyl)benzamide | HCID 23658777 | 53% |
Reaction Steps
3-Bromo-N-[(2S)-2-(4-fluorophenyl)-4-oxobutyl]-N-methyl-5-(trifluoromethyl)benzamide (see method 1; 0.14 g, 0.31 mmol) and 4-[(1-azetidin-3-ylpiperidin-4-yl)carbonyl]morpholine (see method 5; 0.11 g, 0.42 mmol) were dissolved in methylene chloride (10 mL) together dry methanol (0.2 mL). To the resultant solution were added DIPEA (0.12 g, 0.94 mmol) and sodium triacetoxyborohydride (0.13 g, 0.63 mmol). The mixture was stirred under nitrogen for 4 h at RT. The mixture was diluted with methylene chloride and washed twice with saturated aqueous NaHCO3 and then with brine. The organic phase was filtered through a phase separator and the solvent was removed by evaporation. The product was purified by chromatography on silica gel (methanol-methylene chloride, 10:1). There was obtained 0.11 g (53%) of the title compound as a white foam. 1H NMR (500 MHz, CDCl3): δ 1.4-3.8 (cm, 32H), 6.8-7.4 (cm, 6H), 7.7 (s, 1H); LCMS: m/z 684 (M+1)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08106208B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-a518c5e7e82b44878e6031252a44bea4 |
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| Source note | uspto-grants-2012_01 |
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