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HRID 253751作成日:2026年10月27日

Hydroxide → HCID 86642595、化合物

https://huagongshe.com/reaction/253751

反応式

関与物質

役割名称HCID仕込み量
反応物HydroxideHCID 961—
反応物cis-5-chloro-2,3,3a,12b-tetrahydro-2-methyl-1H-dibenz-[2,3:6,7]oxepino[4,5-c]pyrrol-1-oneHCID 56960600—
反応物(3aS,12bS)-5-chloro-2-methyl-2,3,3a,12b-tetrahydro-1H-dibenzo[2,3:6,7]oxepino[4,5-c]pyrrol-1-oneHCID 58729182—
溶媒EthanolHCID 702—
生成物HCID 86642595HCID 8664259522%

反応手順

The mixture of lactams (VII) and (VIII) (13.6 grams, 45 mmol, trans/cis ratio 1:2.3), obtained as described under E, was dissolved in ethanol (140 ml). To the solution postassium hydroxide was added (43 grams, 811 mmol), whereupon the mixture was heated to reflux for 18 hours. Part of the ethanol (60 ml) was evaporated and water was added (200 mL). The aqueous phase was extracted twice with toluene (100 ml ). Subsequently toluene (100 ml) was added to the water phase, followed by concentrated hydrochloric acid to adjust the pH to 1. During the addition of hydrochloric acid the temperature rises to 75° C. The water layer was separated and upon cooling the product crystallized. The crystals were collected by filtration and dried to provide trans-2-chloro-10,11-dihydro-11[(methylamino)methy]-dibenz[b,f]oxepin-10-carboxylic acid hydrochloride (11)(3.75 grams, 10.6 mmol, 22%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07872147B2
出典データセットuspto-grants-2011_01
ORD IDord-26152e3b38f64fb19a4ccd3bf167916b
出典メモuspto-grants-2011_01