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ChemicalBook CAS DataBase List ethyl 2-chloro-4-ethoxy-nicotinate
127423-61-4

ethyl 2-chloro-4-ethoxy-nicotinate synthesis

7synthesis methods
-

Yield: 100%

Reaction Conditions:

with triethylamine in dichloromethane at 20;Cooling with ice;

Steps:

20.1
Example 20. N-(4-(4-amino-l-((S)-pyrrolidin-3-yl)-lH-pyrazolo[3,4-d]pyrimidin-3- yl)phenyl)-3-(trifluoromethyl)benzamide (AD070); Step 1; [0200] (i?)-l-(ter£-butoxycarbonyl)pyrrolidin-3-yl methanesulfonate. A solution of (R)- tert-bntyl 3-hydroxypyrrolidine-l-carboxylate (1.0 g, 5.3 mmol) and triethylamine (2.77 mL, 20 mmol) in CH2Cl2 (20 mL) was cooled in an ice-water bath. To this, methanesulfonyl chloride (1.15 mL, 15 mmol) diluted in CH2Cl2 (10 mL) was added dropwise. The reaction was left stirring for 12 hours at room temperature. Water was added, and organic phases extracted in CH2Cl2 (3x 50 mL), which were subsequently dried onto silica and purified by silica gel chromatography (50% EtOAc:Hexanes to 100% EtOAc gradient) to afford (R)-I- (te/t-butoxycarbonyl)pyrrolidin-3-yl methanesulfonate (1.53 g, brown oil, 100% yield).

References:

THE REGENTS OF THE UNIVERSITY OF CALIFORNIA;DAR, Arvin;SHOKAT, Kevan M. WO2010/45542, 2010, A2 Location in patent:Page/Page column 73