HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 77102Generated: October 26, 2026
N,1-dimethylpyrrolidin-3-amine → HCID 178480456, compound
https://huagongshe.com/reaction/77102
Participants
| Role | Name | HCID | Charge |
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| Reactant | N,1-dimethylpyrrolidin-3-amine | HCID 2758520 | — |
| Reactant | Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 9886157 | — |
| Reactant | HCID 178479749 | HCID 178479749 | — |
| Product | HCID 178480456 | HCID 178480456 | 30% |
Reaction Steps
Method J—Step a To a mixture of 1-[3-(5-Chloro-1H-benzoimidazol-2-yl)-4-fluoro-phenyl]-piperidine-4-carboxylic acid hydrochloride (obtained as described in general method 10, step b) (0.01 g, 0.25 mmol) in dcm (2 mL), HATU (0.10 g, 0.26 mmol), TEA (0.07 mL, 0.55 mmol) and N,N′-dimethyl-3-aminopyrrolidine (0.04 g, 0.31 mmol) were added. The reaction mixture was heated at 35° C. overnight, cooled to room temperature and washed with ammonium chloride solution (2 mL), saturated Na2CO3 solution (2 mL) and water (2 mL). The organic layer was then filtrated on an NH2 cartridge and further purified by flash chromatography (eluent: EtOAc:NH3 2N in MeOH/9:1) to obtain 0.03 g of the title compound (30%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08835648B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-5a847595c8984844a698703d86c9781a |
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| Source note | uspto-grants-2014_09 |
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