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化驗
97%
形狀
solid
光學活性
[α]20/D -8.0°, c = 4 in methanol
mp
179-186 °C
SMILES 字串
Cl.F[C@@H]1CCNC1
InChI
1S/C4H8FN.ClH/c5-4-1-2-6-3-4;/h4,6H,1-3H2;1H/t4-;/m1./s1
InChI 密鑰
LENYOXXELREKGZ-PGMHMLKASA-N
應用
(R)-(−)-3-Fluoropyrrolidine hydrochloride may be used as a substrate in the preparation of:
- Imidazo[1,2-a]pyrazine derivatives as possible aurora kinase inhibitors.
- Pyrazolopyrimidine derivatives as possible PDE10A Inhibitors.
訊號詞
Warning
危險分類
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
標靶器官
Respiratory system
儲存類別代碼
11 - Combustible Solids
水污染物質分類(WGK)
WGK 3
閃點(°F)
Not applicable
閃點(°C)
Not applicable
個人防護裝備
dust mask type N95 (US), Eyeshields, Gloves
Aurora kinase inhibitors based on the imidazo[1, 2-a] pyrazine core: fluorine and deuterium incorporation improve oral absorption and exposure
Journal of Medicinal Chemistry, 54(1), 201-210 (2011)
Scalable Process Design for a PDE10A Inhibitor Consisting of Pyrazolopyrimidine and Quinoxaline as Key Units
Organic Process Research & Development, 23(4), 578-587 (2019)
Bioorganic & medicinal chemistry letters, 14(5), 1265-1268 (2004-02-26)
Amides derived from fluorinated pyrrolidines and 4-substituted cyclohexylglycine analogues have been prepared and evaluated as inhibitors of dipeptidyl dipeptidase IV (DP-IV). Analogues which incorporated (S)-3-fluoropyrrolidine showed good selectivity for DP-IV over quiescent cell proline dipeptidase (QPP). Compound 48 had good
Discovery of a pyrazolo [1, 5-a] pyrimidine derivative (MT-3014) as a highly selective PDE10A inhibitor via core structure transformation from the stilbene moiety
Bioorganic & Medicinal Chemistry, 27(15), 3440-3450 (2019)
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