HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 736932Generated: October 30, 2026
Dimethylformamide → HCID 68591547, compound
https://huagongshe.com/reaction/736932
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 3-(Piperidin-4-yl)-4,5-dihydro-1H-benzo[d][1,3]diazepin-2(3H)-one | HCID 11379587 | — |
| Reactant | HCID 68591454 | HCID 68591454 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68591547 | HCID 68591547 | — |
Reaction Steps
1.8 g (11.0 mmol) CDT were added to a solution of 3.2 g (10.2 mmol) of ethyl (R)-2-amino-3-(4-amino-3-chloro-5-trifluoromethyl-phenyl)-propionate and 1.8 mL (10.3 mmol) ethyldiisopropylamine in 150 mL THF cooled to 0° C. and the reaction mixture was stirred for 45 min at this temperature and after removal of the ice bath stirred for a further 30 min. Then 2.5 g (10.2 mmol) 3-piperidin-4-yl-1,3,4,5-tetrahydro-1,3-benzodiazepin-2-one suspended in 50 mL THF were added. 40 mL DMF were added to the reaction solution and this was stirred for 2 h at 80° C. It was evaporated down i.vac., combined with 200 mL EtOAc and 200 mL 10% citric acid solution, the organic phase was separated off, extracted with 150 mL NaHCO3 solution and dried over Na2SO4. After elimination of the desiccant and solvent the desired product was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07595312B2 |
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| Source dataset | uspto-grants-2009_09 |
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| ORD ID | ord-62e6d74260734c91b97dbebf82fe58a7 |
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| Source note | uspto-grants-2009_09 |
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