ChemicalBook CAS DataBase List tert-butyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)piperidine-1-carboxylate

tert-butyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)piperidine-1-carboxylate synthesis

6synthesis methods

Product Name:tert-butyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)piperidine-1-carboxylate
CAS Number:1048970-17-7
Molecular formula:C16H30BNO4
Molecular Weight:311.22

1,2,3,6-TETRAHYDROPYRIDINE-4-YL-BORONIC ACID PINACOL ESTER

375853-82-0

tert-butyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)piperidine-1-carboxylate

1048970-17-7

General procedure for the synthesis of 1-N-tert-butoxycarbonylpiperidine-4-boronic acid pinacol ester from 1,2,3,6-tetrahydro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine: method 4: general conditions for the reduction of tetrahydropyridines to piperidines in the presence of boronic acid ester: the boronic acid ester was dissolved in a mixed solvent of ethyl acetate and methanol (1:1 v/v) , with a final borate concentration of 0.4 M) in a mixture of ethyl acetate and methanol, followed by the addition of palladium hydroxide (0.35 equiv). The reaction mixture was stirred under hydrogen atmosphere for 14 hours. Upon completion of the reaction, the reaction mixture was filtered and concentrated in vacuum to give the target piperidine product in quantitative yield. Example 8: Piperidine 8 was prepared from compound 1 in a two-step reaction using Method 4, followed by deprotection of pinacol esters using Method 2. [M-H]? = 228.2 m/z. activity: b

76-09-5 Synthesis

76-09-5
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180695-79-8 Synthesis

180695-79-8
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274-07-7
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$78.09/5g

1048970-17-7
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$11.00/250mg

Yield:1048970-17-7 36%

Reaction Conditions:

Stage #1:benzo[1,3,2]dioxaborole with bis(cyclopentadienyl)titanium dichloride;potassium carbonate in tert-butyl methyl ether for 0.5 h;
Stage #2:tert-butyl 4-bromo-1-piperidinecarboxylate in tert-butyl methyl ether at 80; under 760.051 Torr; for 24 h;Inert atmosphere;
Stage #3:2,3-dimethyl-2,3-butane diol with triethylamine in tert-butyl methyl ether at 20; for 1 h;Inert atmosphere;

Steps:

80 Example 80
bis(cyclopentadiene)titanium dichloride (denoted as Cp2TiCl2, 0.01mmol, 2.5mg), potassium carbonate (denoted as K2CO3, 0.2mmol, 26.7mg), methyl tert-butyl ether (1mL) Add catecholborane (denoted as HBcat, 0.6mmol, 63μL) into a 38mL pressure tube in sequence, stir for 30min and then add 1-Boc-4-bromopiperidine (denoted as 1ao, 0.2mmol,53mg) in nitrogen Stir at 80°C for 24h under a (1atm) atmosphere, add triethylamine (0.6mmol, 84μL) and pinacol (0.6mmol, 70.8mg) after the reaction, and stir at room temperature for 1h. Then use petroleum ether/ethyl acetate (20:1, v/v) as the eluent to carry out column chromatography purification to obtain the structure compound represented by formula 2ao (colorless and transparent liquid, 1-tert-butyl carboxylate-2-(4) ,4,5,5-Tetramethyl-1,3,2-dioxaborocyclyl)piperidine). The isolated yield is 36%.

References:

CN112645971, 2021, A Location in patent:Paragraph 0229-0231

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