HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 337318Generated: October 30, 2026
3,3-Difluoroazetidine hydrochloride → HCID 86676936, compound
https://huagongshe.com/reaction/337318
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3,3-Difluoroazetidine hydrochloride | HCID 2758247 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | HCID 86662317 | HCID 86662317 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | HCID 86676936 | HCID 86676936 | — |
Reaction Steps
To a solution of 2-(6-(6-chloro-2-methyl-3-oxo-2,3-dihydropyridazin-4-ylamino)pyridin-3-yloxy)-2-methylpropanal (665 mg, 2.06 mmol, Eq: 1.00) in DCE (70 ml) was added 3,3-difluoroazetidine hydrochloride (347 mg, 2.68 mmol, Eq: 1.30). The mixture was stirred at RT for 1 h, then sodium triacetoxyborohydride (655 mg, 3.09 mmol, Eq: 1.5) was added and stirring was continued for 18 h. The reaction mixture was diluted with saturated NaHCO3 solution and extracted with DCM (5×20 mL). The organic layer was dried (MgSO4) and concentrated in vacuo. The resultant residue was purified by chromatography (SiO2-50 g, Hex:AcOEt, 7:3 in 20 min, then 50% in 30 min) to afford the desired product (566 mg) as a white powder. (M+H)+=400 m/e. 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 1.29 (s, 6 H) 2.79 (br. s., 2 H) 3.70-3.81 (m, 4 H) 3.83 (s, 3 H) 6.87 (dd, J=8.84, 0.51 Hz, 1 H) 7.32 (d, J=8.59 Hz, 1 H) 8.10 (d, J=2.78 Hz, 1 H) 8.22 (s, 1 H) 8.28 (s, 1 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08889682B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-2b66718296b847b9a893cc773af58317 |
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| Source note | uspto-grants-2014_11 |
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