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184968-86-3

1-Boc-4-(2-thioxopiperidin-1-ylMethyl)piperidine synthesis

5synthesis methods
184968-83-0 Synthesis
1-Boc-4-(2-oxo-piperidin-1-ylMethyl)piperidine

184968-83-0
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1-Boc-4-(2-thioxopiperidin-1-ylMethyl)piperidine

184968-86-3
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Yield:184968-86-3 82%

Reaction Conditions:

with Lawessons reagent in tetrahydrofuran at 23; for 20 h;

Steps:

2.3.2C Prep. 2C:

Combine the product (1.50 g, 5.06 mmol) of Prep. 2A and Lawesson reagent (1.13 g, 2.78 mmol) in dry THF (20 mL) under N2. Stir at 23°C for 20 h. Concentrate and purify by chromatography (200 mL of flash silica gel; eluant: 1:3 EtOAc:hexane, 1:2 EtOAc:hexane, then 1:1 EtOAc:hexane). Combine appropriate fractions and concentrate to give 1.30 g (4.16 mmol, 82%) as a green oil. MS (FAB): m/e 313 (M+1).

References:

EP1032561,2004,B1 Location in patent:Page 12

123855-51-6 Synthesis
N-Boc-4-piperidinemethanol

123855-51-6
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1-Boc-4-(2-thioxopiperidin-1-ylMethyl)piperidine

184968-86-3
1 suppliers
inquiry