Triethylamine → Abecarnil

Temperature

-15 °C

A solution is prepared from 3.3 g (8.5 mmol) of 6-benzyloxy-4-methoxymethyl-l,2,3,4-tetrahydro-β-carboline-3-carboxylic acid isopropyl ester in 150 ml of methylene chloride, combined under argon with 3.9 ml of triethylamine, and cooled to -15° C. At this temperature, a solution of 3.2 ml (25.6 mmol) of tert-butyl hypochlorite in 50 ml of methylene chloride is added dropwise without delay to this solution. After the adding step is completed, the mixture is stirred for another 10 minutes, combined with 2.6 ml of triethylamine, and agitated for 2 hours at room temperature. Subsequently, the mixture is concentrated to one-half thereof and extracted once by shaking with dilute ammonia solution. The organic phase is dried, filtered, and concentrated. The residue is chromatographed over silica gel with methylene chloride:acetone =4:1 as the eluent. Recrystallization from ethyl acetate gives 1.1 g (35% yield) of 6-benzyloxy-4-methoxymethyl-β-carboline-3-carboxylic acid isopropyl ester, mp 150°-151° C.

1. stirringagitated for 2 hours at room temperature
2. concentrationSubsequently, the mixture is concentrated to one-half
3. extractionextracted once
4. stirringby shaking with dilute ammonia solution
5. customThe organic phase is dried
6. filtrationfiltered
7. concentrationconcentrated
8. customThe residue is chromatographed over silica gel with methylene chloride
9. customRecrystallization from ethyl acetate

ORD record

ord-a4c300292c194c209d106ac002599916

Source dataset

uspto-grants-1997_12

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US05700808