Methanol → HCID 56829411、化合物

To a stirred suspension of cis-4-(4-fluorophenoxy)-L-proline (which can be prepared as set forth by Ondetti et al. in Example 36 of U.K. patent application No. 2,028,327) (250 mg., 11 mmole) in 70 ml. of methanol at -30° under argon, there is added 8.09 ml. (10 eq.) of thionyl chloride. After stirring at -20° for 2 hours, the cold bath is removed and the mixture is stirred at room temperature for 16 hours. The solvent is removed at reduced pressure and the residue is dissolved in 150 ml. of dichloromethane. The resulting solution is washed with 1N sodium bicarbonate (twice) and water. After drying (MgSO4), the solution is treated with excess hydrochloric acid and then concentrated at reduced pressure. Recrystallization from methanol/ether gives 1.49 g. of product. The mother liquors yield an additional 0.5 g. of product so that a total of 1.99 g. of cis-4-(4-fluorophenoxy)-L-proline, methyl ester, hydrochloride is obtained; m.p. 147°-148° (s. 144°); [α]D20 =+6.96° (c=1.55, methanol).

1. customcan be prepared
2. customthe cold bath is removed
3. stirringthe mixture is stirred at room temperature for 16 hours
4. customThe solvent is removed at reduced pressure
5. dissolutionthe residue is dissolved in 150 ml
6. washThe resulting solution is washed with 1N sodium bicarbonate (twice) and water
7. dry with materialAfter drying (MgSO4)
8. additionthe solution is treated with excess hydrochloric acid
9. concentrationconcentrated at reduced pressure
10. customRecrystallization from methanol/ether
11. customgives 1.49 g
12. customThe mother liquors yield an additional 0.5 g

ORDレコード

ord-7aaa199f34af430cb81074869d9d3054

出典データセット

uspto-grants-1984_07

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US04462943