|
| Carbamic acid, [(1S,3S)-3-aminocyclopentyl]-, 1,1-dimethylethyl ester (9CI) Basic information |
Product Name: | Carbamic acid, [(1S,3S)-3-aminocyclopentyl]-, 1,1-dimethylethyl ester (9CI) | Synonyms: | Carbamic acid, [(1S,3S)-3-aminocyclopentyl]-, 1,1-dimethylethyl ester (9CI);tert-butyl ((1S,3S)-3-aminocyclopentyl)carbamate;Carbamic acid, N-[(1S,3S)-3-aminocyclopentyl]-, 1,1-dimethylethyl ester;tert-butyl N-[(1S,3S)-3-aminocyclopentyl]carbamate;[(1S,3S)-3-Amino-1-(boc-amino)cyclopentane;TERT-BUTYL ((IS, 3S)-3- AMINOCYCLOPENTYL)CARBAMATE | CAS: | 645400-44-8 | MF: | C10H20N2O2 | MW: | 200.28 | EINECS: | | Product Categories: | N-BOC;CYCLOPENTANE | Mol File: | 645400-44-8.mol | |
| Carbamic acid, [(1S,3S)-3-aminocyclopentyl]-, 1,1-dimethylethyl ester (9CI) Chemical Properties |
Boiling point | 304.2±31.0 °C(Predicted) | density | 1.04±0.1 g/cm3(Predicted) | storage temp. | Keep in dark place,Inert atmosphere,Room temperature | pka | 12.37±0.40(Predicted) |
| Carbamic acid, [(1S,3S)-3-aminocyclopentyl]-, 1,1-dimethylethyl ester (9CI) Usage And Synthesis |
Uses | tert-butyl N-[(1S,3S)-3-aminocyclopentyl]carbamate is used as a reactant in the synthesis of C-2 hydroxyethyl imidazopyrrolo pyridines as JAK1 inhibitors. | Synthesis | A flask containing tert-butyl [(1S,3S)-3-aminocyclopentyl]carbamate (16.5 g, crude ~0.05 mol) and 1.7 g Pd-C (10% paste) in MeOH (300 mL) was exposed to a positive pressure of hydrogen gas (balloon) over weekend. The catalyst was filtered off and the mixture was concentrated to afford the title compound (9.5 g) as a thick colorless viscous oil. Tert-butyl [(1S,3S)-3-aminocyclopentyl]carbamate, Yield (9.5 g) |
| Carbamic acid, [(1S,3S)-3-aminocyclopentyl]-, 1,1-dimethylethyl ester (9CI) Preparation Products And Raw materials |
|