반응 #744203

반응 방정식

NaHCO3

NaBH(OAc)3

(6-chloro-1-oxido-3-oxo-1,2,4-benzotriazin-4(3H)-yl)acetaldehyde

1,1-dimethylethyl (2,3-dihydro[1,4]dioxino[2,3-c]pyridin-7-ylmethyl)-4-piperidinylcarbamate

→

desired compound

수율 42.0%

1,1-Dimethylethyl {1-[2-(6-chloro-1-oxido-3-oxo-1,2,4-benzotriazin-4(3H)-yl)ethyl]-4-piperidinyl}(2,3-dihydro[1,4]dioxino[2,3-c]pyridin-7-ylmethyl)carbamate

수율 42.0%

용매

MeOH

chloroform

반응 조건

후처리

1. 1
   추출The reaction was then extracted with 10% MeOH in DCM (3×200 ml)
2. 2
   기타The combined organic phases were dried
3. 3
   기타evaporated
4. 4
   기타the crude residue purified by chromatography on silica gel using a 0-10% MeOH/DCM gradient

실험 절차

A mixture of (6-chloro-1-oxido-3-oxo-1,2,4-benzotriazin-4(3H)-yl)acetaldehyde (89 mg, 0.372 mmol) and 1,1-dimethylethyl (2,3-dihydro[1,4]dioxino[2,3-c]pyridin-7-ylmethyl)-4-piperidinylcarbamate (for a synthesis see WO2004/058144 Example 99(h)) (117 mg, 0.334 mmol) in chloroform (5 ml) and MeOH (0.5 ml) was stirred for 2 h before addition of NaBH(OAc)3 (212 mg, 1.002 mmol). The reaction was stirred for 1 h before addition of sat. aq NaHCO3 (50 ml). The reaction was then extracted with 10% MeOH in DCM (3×200 ml). The combined organic phases were dried, evaporated and the crude residue purified by chromatography on silica gel using a 0-10% MeOH/DCM gradient to provide the desired compound as a yellow oil (81 mg, 42%).

출처