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ChemicalBook CAS DataBase List 1-Piperidinecarboxylic acid, 3-[[(phenylmethoxy)carbonyl]amino]-, 1,1-dimethylethyl ester, (3R)-
320580-76-5

1-Piperidinecarboxylic acid, 3-[[(phenylmethoxy)carbonyl]amino]-, 1,1-dimethylethyl ester, (3R)- synthesis

2synthesis methods
188111-79-7 Synthesis
(R)-1-Boc-3-Aminopiperidine

188111-79-7
358 suppliers
$6.00/1g

1-Piperidinecarboxylic acid, 3-[[(phenylmethoxy)carbonyl]amino]-, 1,1-dimethylethyl ester, (3R)-

320580-76-5
41 suppliers
inquiry

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Yield:320580-76-5 78.0 %

Reaction Conditions:

with N-ethyl-N,N-diisopropylamine in tetrahydrofuran at 25;

Steps:

Step (a): preparation of tert-butyl (3R)-3-(benzyloxycarbonylamino)piperidine-1-carboxylate (compound C1.2)

To a solution of tert-butyl (3R)-3-aminopiperidine-1-carboxylate (compound C1.1, 10.0 g, 49.9 mmol) in THF (200 mL) was added Cbz-OSu (14.9 g, 59.9 mmol) and DIEA (9661.5 mg, 74.9 mmol), the resultant mixture was stirred at 25 °C for 2 hrs. The reaction was quenched with N HCl (aq. 50 mL), and extracted with EA (50 mL) for three times. The combined organic layer was washed with brine, dried over Na2SO4, filtered and concentrated. The residue was purified by column chromatography (silica gel, 20% to 50% EA in PE) to afford compound C1.2 (13.0 g, 78.0 % yield). MS: calc'd 335 [(M+H)+]; measured 357, [(M+Na)+],

References:

WO2022/243346,2022,A1 Location in patent:Page/Page column 35

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