“…J-E C32H36N202S-2HC1 C,6 H, Cl, N °A, Me2CO; B, SkellysolveB; C,n-BuOH; D, EtOH; E,H20; F, C6H6; G, CH2C12; H, EtOAc; I,CHC13; J, GPrOH. 6 Anal, results for indicated elements are within ±0.4% of the theor values unless otherwise noted. c Cf.…”
supporting
confidence: 51%
“…The N02 group then was modified through reduction and subsequent acylation to yield benzo [b]thiophenes 3i-3j. Scheme II is related to work by Middleton in which 2-carboxy-substituted benzo [b]thiophenes were prepared from the reaction of mercaptoacetic acid with 2-chloro-5-nitrobenzophenone followed by cyclization.10 It was hoped that the 5aminobenzo [b ¡thiophene 3i might serve as a precursor to the 5-OH-substituted relative which had proved (8) Similar syntheses of benzo [6 ]thiophenes have been reported previously. Cf.…”
mentioning
confidence: 84%
“…A series of 2,3-diarylbenzo [6 ]furans has been reported by Grover, et al,n to possess antifertility activity. A similar series of compounds was synthesized independently in these laboratories111 using a synthetic approach (cf.…”
Syntheses and biological activities are reported for 24 of the title compds. The most active compds were 6-methoxy-3-{p-[2-(1-pyrrolidyl )ethoxy] phenyl | -2-phenylbenzo [b] thiophene (3m) and 3,4-dihydro-7-methoxy-3-phenyl-4-hydroxy-4-{p-[2-(l-pyrrolidyl)ethoxy]phenyl}-lJ7-2-benzothiapyran (11a). In addition to the title compds, a dibenzo[b,e]thiepin (20) containing some of the structural features of 11a is reported; this structural modification resulted in loss of activity. Both 3m and 11a afford complete protection against pregnancy in rats at doses of 0.1 mg/kg. The compds exhibit a rapidly plateauing uterotropic activity in the rat which does not approach the maxima seen with known potent estrogens.
“…J-E C32H36N202S-2HC1 C,6 H, Cl, N °A, Me2CO; B, SkellysolveB; C,n-BuOH; D, EtOH; E,H20; F, C6H6; G, CH2C12; H, EtOAc; I,CHC13; J, GPrOH. 6 Anal, results for indicated elements are within ±0.4% of the theor values unless otherwise noted. c Cf.…”
supporting
confidence: 51%
“…The N02 group then was modified through reduction and subsequent acylation to yield benzo [b]thiophenes 3i-3j. Scheme II is related to work by Middleton in which 2-carboxy-substituted benzo [b]thiophenes were prepared from the reaction of mercaptoacetic acid with 2-chloro-5-nitrobenzophenone followed by cyclization.10 It was hoped that the 5aminobenzo [b ¡thiophene 3i might serve as a precursor to the 5-OH-substituted relative which had proved (8) Similar syntheses of benzo [6 ]thiophenes have been reported previously. Cf.…”
mentioning
confidence: 84%
“…A series of 2,3-diarylbenzo [6 ]furans has been reported by Grover, et al,n to possess antifertility activity. A similar series of compounds was synthesized independently in these laboratories111 using a synthetic approach (cf.…”
Syntheses and biological activities are reported for 24 of the title compds. The most active compds were 6-methoxy-3-{p-[2-(1-pyrrolidyl )ethoxy] phenyl | -2-phenylbenzo [b] thiophene (3m) and 3,4-dihydro-7-methoxy-3-phenyl-4-hydroxy-4-{p-[2-(l-pyrrolidyl)ethoxy]phenyl}-lJ7-2-benzothiapyran (11a). In addition to the title compds, a dibenzo[b,e]thiepin (20) containing some of the structural features of 11a is reported; this structural modification resulted in loss of activity. Both 3m and 11a afford complete protection against pregnancy in rats at doses of 0.1 mg/kg. The compds exhibit a rapidly plateauing uterotropic activity in the rat which does not approach the maxima seen with known potent estrogens.
“…It was shown in the early 1960's by Perelman and co-workers [59] and by Fried and associates [74] that the introduction of a A 4>9 -bisdehydro system in the 19-norsteroids resulted in the preparation of exceptionally potent oral antiestrogens. These compounds could be synthesized by a one-step bromination of A 5(10) -3-ketosteroids in pyridine solution (as illustrated in the conversion of 55 to 57, Scheme 10-5).…”
“…Compared with 17a-ethinyl-19-nortestosterone, its L15-10 analogue (Enovid) had 2-3 times more anti-gonadotropin potency, but only 0.1 times the progestational potency. A number of 17a-trifluoropropynyl or 17a-trifl.uorovinyl androstene derivatives have been described which possess both types of biological activity (FRIED et al, 1961).…”
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