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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1621302Generated: November 3, 2026

Water → 3-[7-Chloro-2-(4-methoxy-benzyl)-1-oxo-1,2-dihydro-isoquinolin-6-yloxy]-8-aza-bicyclo[3.2.1]octane-8-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1621302

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactanttert-Butyl 3-hydroxy-8-azabicyclo(3.2.1)octane-8-carboxylateHCID 21187725—
Reactant7-Chloro-6-fluoro-2-[(4-methoxyphenyl)methyl]isoquinolin-1(2H)-oneHCID 59818247—
SolventDimethylacetamideHCID 31374—
Product3-[7-Chloro-2-(4-methoxy-benzyl)-1-oxo-1,2-dihydro-isoquinolin-6-yloxy]-8-aza-bicyclo[3.2.1]octane-8-carboxylic acid tert-butyl esterHCID 6702285580.1%

Reaction Steps

528 mg of sodium hydride (60%) were suspended in 8 mL of dimethyl acetamide and 1.00 g of 3-hydroxy-8-aza-bicyclo[3.2.1]octane-8-carboxylic acid tert-butyl ester (70), dissolved in 4 mL of dimethyl acetamide, were added dropwise. After 1 h, 1.40 g of 7-Chloro-6-fluoro-2-(4-methoxy-benzyl)-2H-isoquinolin-1-one (62), dissolved in another 8 mL of dimethyl acetamide, were added. The reaction mixture was stirred at room temperature until the reaction was complete. 30 mL of water were added, the resulting suspension extracted three times with a mixture of dichloromethane and 2-propanol (3:1) and the combined organic layers were evaporated. Water was added and the crude product was subjected to lyophilization to remove remainders of dimethyl acetamide. The obtained crude product was purified by silica gel chromatography to yield 1.85 g of the title compound as a mixture of diastereoisomers (71). Rt=1.95 min, 2.03 min (Method C). Detected mass: 525.0 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772492B2
Source datasetuspto-grants-2014_07
ORD IDord-bf6d0eddf15b47dfa383d9f3ec55c17f
Source noteuspto-grants-2014_07