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CAS No. : | 5382-17-2 | MDL No. : | MFCD00035298 |
Formula : | C5H12ClNO | Boiling Point : | No data available |
Linear Structure Formula : | - | InChI Key : | VKCORPXOKYDINR-UHFFFAOYSA-N |
M.W : | 137.61 | Pubchem ID : | 16212499 |
Synonyms : |
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Signal Word: | Warning | Class: | |
Precautionary Statements: | P261-P305+P351+P338 | UN#: | |
Hazard Statements: | H315-H319-H335 | Packing Group: | |
GHS Pictogram: |
* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In DMF (N,N-dimethyl-formamide); at 20℃; for 16.0h; | To a stirred solution OF BOC-3- (4-FLUOROPHENYL)- (S)-ALANINE (LO. OG, 35. 3MMOL), <strong>[5382-17-2]4-hydroxypiperidine hydrochloride</strong> (5. 1G, 37. 1MMOL) and HOBt (7.2g, 52. 9MMOL) in DMF (lOOmL), was added DIPEA (12. 3mL, 70. 6MMOL) and after 5MIN, EDCI (7.4g, 38. 8MMOL) and the reaction stirred at rt for 16H. The solvent was removed in vacuo and the residue partitioned between water (150ML) and ethyl acetate (2 x 150ML). The combined organic fractions were washed with sodium hydroxide solution (2M, 50ML), hydrochloric acid (2N, 50ML), dried (MGS04) and concentrated in vacuo. The product was chromatographed on silica gel eluting with ethyl acetate to give the title compound as a white solid. m/z (ES+) = 367 [M+ H] + ; RT = 3.28min. |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With sodium carbonate; In dichloromethane; water; at 0℃; for 1.08333h; | Preparation 11: 4-Hydroxypiperidine-l-carbonitrileA stirred slurry OfNa2CO3 (9.8 g, 117 mmol) in water (15 mL) was cooled on ice-water and 4-hydroxypiperidine.HCl (4.0 g, 29.2 mmol) was added. A solution of cyanogen bromide(3.7 g, 35 mmol) in CH2Cl2 (90 mL) was added portionwise over 5 min and the stirring continued for 1 h. The reaction was diluted with CH2Cl2 ( 100 mL), the organic phase separated and dried (MgSO-O and the solvent evaporated to afford the title cyanamide: SH (CDCl3) 1.65 (ddt, 2H), 1.91 (ddt, 2H), 2.17 (br s, IH), 3.08 (ddd, 2H), 3.45 (ddd, 2H), 3.86 (sept, IH). |
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