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2-Cyclopentylthiazole-5-carbaldehyde synthesis

5synthesis methods
1494277-04-1 Synthesis
(2-Cyclopentylthiazol-5-yl)methanol

1494277-04-1
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2-Cyclopentylthiazole-5-carbaldehyde

1251104-23-0
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Yield: 87%

Reaction Conditions:

with Dess-Martin periodane in dichloromethane at 0 - 30; for 5 h;

Steps:

16.5 Step 5
To a mixture of 25e (2.1 g, 11.4 mmol) in DCM (50 mL) was added DMP (4.7 g, 12.5 mmol) in portions with stirring at 0 °C and then stirred at 30°C for 5 hours, before the mixture was quenched with Sat Na2S03 solution. After filtration and concentration in vacuo, and the resutling residue was purified using Si02 chromatography, eluting with petroleum ether: ethyl acetate (100/1-10/1) to provide25f (1.8 g, 87%). 1H NMR (CDC13) δ: 9.96 (s, 1H), 8.26 (s, 1H), 3.47 (q, J=7.7 Hz, 1H), 2.23 - 2.14 (m, 2H), 1.87 - 1.79 (m, 4H), 1.71 (s., 2H)

References:

MERCK SHARP & DOHME CORP.;YU, Wensheng;TONG, Ling;KOZLOWSKI, Joseph A.;SELYUTIN, Oleg;CHEN, Lei;KIM, Jae-Hun;SHA, Deyou;RIZVI, Razia;SHANKAR, Bandarpalle;HU, Bin;ZHONG, Bin;WAI, Dahai;HAO, Jinglai;WEI, Wei;JI, Tao;ZAN, Shuai WO2014/110705, 2014, A1 Location in patent:Page/Page column 85-86

42202-73-3 Synthesis
CYCLOPENTANECARBOTHIOAMIDE

42202-73-3
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2-Cyclopentylthiazole-5-carbaldehyde

1251104-23-0
8 suppliers
inquiry