Morphanthridines II. 11‐aminoalkyl‐5,6‐dihydromorphanthridines

Drukker, Alexander E.; Judd, Claude I.; and, Joan M. Spoerl; Kaminski, Frank E.

doi:10.1002/jhet.5570020312

“…5,6-Dihydro-l1 -hydroxy-5-methyl-6-oxomorphanthridine. Sodium borohydride (4 g) was added in portions to a stirred, cooled suspension of 5,6-dihydro-5-methyl-6,11dioxomorphanthridine (Drukker & Judd, 1965) (10 g) in methanol (200 ml), the temperature being kept below 10". The mixture was stirred for 1 h at 10-15", diluted with water (150 ml), acidified with dilute hydrochloric acid and filtered.…”

Section: Methods Dmentioning

confidence: 99%

Basic dihydromorphanthridinones with anticonvulsant activity

Waring¹,

Whittle²

1969

Journal of Pharmacy and Pharmacology

6

0

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“…The anion was generated with sodamide in refluxing toluene (16). We have found that the sodium salt is more conveniently generated with sodium hydride in dimethyl formamide at room temperature.…”

Section: -Methyl-56-diliydro-11mentioning

confidence: 99%

Dibenzo[a,d]cycloheptene and related compounds. II. The synthesis of some 11-substituted dibenzo[b,e]azepin-6-one, 5-substituted dibenzo[a,d]cycloheptene, and 12-substituted dibenzo[a,d]cyclooctene derivatives

Ackermann¹,

Chapuis²,

Horning³

et al. 1969

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“…

Because of our interest in the preparation of basic substituted morphanthridines (1,2 ) , we have investigated the Bischler-Napieralski cyclization of 2-acylaminobenzophenones in an effort to obtain the useful intermediates, 11morphanthridones. This cyclization method was applied quite successfully for the preparation o€ 6substituted morphanthridines from 2acylaminodiphenylmethanes (3,4), a s well a s for the synthesis of related oxazepines and thiazepines (4, 5).However, when we treated 2formylamino-5chlorobenzophenone (la) with hot polyphosphoric acid, only 2 -amino -5chlorobenzophenone was isolated.

…”

mentioning

confidence: 99%

A new synthesis of anilinoquinolines. Morphanthridines IV

Drukker

¹

,

Judd

²

1966

Journal of Heterocyclic Chem

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Because of our interest in the preparation of basic substituted morphanthridines (1,2 ) , we have investigated the Bischler-Napieralski cyclization of 2-acylaminobenzophenones in an effort to obtain the useful intermediates, 11morphanthridones. This cyclization method was applied quite successfully for the preparation o€ 6substituted morphanthridines from 2acylaminodiphenylmethanes (3,4), a s well a s for the synthesis of related oxazepines and thiazepines (4, 5).However, when we treated 2formylamino-5chlorobenzophenone (la) with hot polyphosphoric acid, only 2 -amino -5chlorobenzophenone was isolated. This is in agreement with the reported recovery of 2-aminodiphenylmethane from the attempted polyphosphoric acid cyclization of its 2fonnylamino analog, a s reported by Jilek, et al. (3). Heating the 2acetylaminoketone (Ib) with polyphosphoric acid resulted in the formation in high yield of a bright yellow crystalline solid, Neither the analytical nor the spectral data of the product were in agreement with those for the expected 11-morphanthridone (11). The elemental assay indicated an empirical formula C28H&12N20, while its infrared spectrum was notably lacking in extinctions in the 3.3 to 3.6 p region, indicating the absence of methyl-and methylene groups. This was confirmed by its nuclear magnetic resonance spectrum.Furthermore, the compound showed a carbonyl absorption a t 6.12 p , which is in the same position as a carbonyl absorption of its precursor Ib, but which had only approximately half its intensity. Comparison of the ultraviolet spectra of the compound in alcohol and in alcohol containing 0.1 N hydrochloric acid, showed a shift to shorter wave-length in the latter case (Table I). All this evidence suggested that the cyclization product was the benzoylanilinoquinoline 111. A possible reaction mechanism involves acid catalyzed aldol cyclization concomitant with anil formation with the simultaneously formed benzoylaniline (6).Structure proof of 111 a s well a s added support for the proposed mechanism was obtained by an alternate synthesis. Base catalyzed cyclization of the acetylaminobenzophenone Ib according to the method of Hauser (7) afforded 6-chloro-4-phenylcarbostyril (IV) (a), which when treated with phosphorus oxychloride (9) yielded 2,6-dichloro-Pphenylquinoline (V). This was then made to react with 2-amino -5chlorobenzophenone in order to afford III. Comparison of the infrared spectrum of m with that of the cyclization product, as well a s lack of depression of their mixture melting points, proved the compounds to be identical.A s expected, similar cyclization of Z-propionylamino-5-chlorobenzophenone afforded the 3-methyl analog of III. TABLE I Ultraviolet Spectra, x max. IU/.I (c x I$) Ia (EtOH) III (EtOH) III (EtOH + 0.1 N HC1) 205-6 (24,5) 222-3 (47.3) 251 (30,6) 238 (24,36) 257-8 (34,8) 368 (9.5) 329 (1.97) 285 (30.6) 343 (5,12) 3 9 2 4 (9,O) M. I a. R = H 0. R = M e I 111 r I b -CI -a CI qc'-III Ph m I V V

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Morphanthridines II. 11‐aminoalkyl‐5,6‐dihydromorphanthridines

Cited by 5 publications

References 9 publications

Basic dihydromorphanthridinones with anticonvulsant activity

Basic dihydromorphanthridinones with anticonvulsant activity

Dibenzo[a,d]cycloheptene and related compounds. II. The synthesis of some 11-substituted dibenzo[b,e]azepin-6-one, 5-substituted dibenzo[a,d]cycloheptene, and 12-substituted dibenzo[a,d]cyclooctene derivatives

A new synthesis of anilinoquinolines. Morphanthridines IV

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