Methanol → 2'-Methyl-2',3'-dihydro-1'H-spiro[cyclopropane-1,4'-isoquinolin]-7'-amine

To a stirred suspension of 2′-methyl-2′,3′-dihydro-1′H-spiro[cyclopropane-1,4′-isoquinolin]-7′-amine dihydrochloride (1.90 kg, 7.27 mol, 1.09 eq.) in chloroform (19 L) at room temperature was added 5 N NaOH (3.8 L), and the mixture was stirred for 5 minutes. The chloroform layer was separated and the aqueous layer was extracted with chloroform (9.5 L). Combined chloroform layers were washed with 5% aqueous NaCl (9.5 L), then dried over anhydrous sodium sulfate (3.8 kg) for 1 hour. Sodium sulfate was filtered and washed with chloroform (3.8 L). Combined filtrate and washing were evaporated to give crude oil. Methanol (4.6 L) was added and the solution was evaporated to give 2′-methyl-2′,3′-dihydro-1′H-spiro[cyclopropane-1,4′-isoquinolin]-7′-amine (1.40 kg) as brownish crystals in crude 102% recovery.

1. customThe chloroform layer was separated
2. extractionthe aqueous layer was extracted with chloroform (9.5 L)
3. washCombined chloroform layers were washed with 5% aqueous NaCl (9.5 L)
4. dry with materialdried over anhydrous sodium sulfate (3.8 kg) for 1 hour
5. filtrationSodium sulfate was filtered
6. washwashed with chloroform (3.8 L)
7. washCombined filtrate and washing
8. customwere evaporated
9. customto give crude oil
10. customthe solution was evaporated

ORD 기록

ord-c45ffa459f6d47f89c20c01eceee5425

출처 데이터셋

uspto-grants-2013_05

DOI

10.6084/m9.figshare.5104873.v1

특허 번호

US08436004B2