(R)-3-FORMYL-3,4-DIHYDRO-1H-ISOQUINOLINE-2-CARBOXYLIC ACID TERT-BUTYL ESTER synthesis
- Product Name:(R)-3-FORMYL-3,4-DIHYDRO-1H-ISOQUINOLINE-2-CARBOXYLIC ACID TERT-BUTYL ESTER
- CAS Number:444583-19-1
- Molecular formula:C15H19NO3
- Molecular Weight:261.32
![2(1H)-Isoquinolinecarboxylic acid, 3,4-dihydro-3-[(methoxymethylamino)carbonyl]-, 1,1-dimethylethyl ester, (3R)-](/CAS/20210305/GIF/444583-18-0.gif)
444583-18-0
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444583-19-1
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Yield:444583-19-1 100%
Reaction Conditions:
with lithium aluminium tetrahydride in tetrahydrofuran;diethyl ether at 0; for 1 h;
Steps:
214.B Step B.; (3R)-tert-Butyl 3-formyl-3,4-dihydroisoquinoline-2(1H)-carboxylate
Lithium aluminum hydride (1 M in THF, 5.3 ml, 5.3 mmol) was added to a solution of (3R)-tert-butyl 3-(methoxy(methyl)carbamoyl)-3,4-dihydroisoquinoline-2(1H)-carboxylate (1.7 g, 5.0 mmol theory) in ether (16 ml) stirring at 0° C. under nitrogen. After stirring at 0° C. for 1 h, the reaction was slowly quenched with water (0.40 ml). Sodium hydroxide (1N, 0.80 ml) followed by water (0.60 ml) were then added and the resultant gelatinous precipitate was filtered through Celite rinsing with ether and THF. The filtrate was evaporated and the residue transferred to a separatory funnel with EtOAc. Washing with brine and drying with MgSO4 afforded crude product (1.3 g, 100% yield) which was used in the next step without further purification
References:
US2005/80074,2005,A1 Location in patent:Page/Page column 72
845543-81-9
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444583-19-1
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24424-99-5
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444583-19-1
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103733-65-9
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$5.00/100mg
444583-19-1
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