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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 329729생성일: 2026년 10월 26일

Triethylamine → 6-chloro-3,4-dihydro-3-oxo-N-[1-(3-phenoxypropyl)-4-piperidyl]-2H-1,4-benzoxazine-8-carboxamide hydrochloride

https://huagongshe.com/reaction/329729

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Ethyl chloroformateHCID 10928—
반응물6-Chloro-3-oxo-3,4-dihydro-2H-1,4-benzoxazine-8-carboxylic acidHCID 14719836—
반응물1-(3-Phenoxypropyl)piperidin-4-amineHCID 14802120—
용매TetrahydrofuranHCID 8028—
생성물6-chloro-3,4-dihydro-3-oxo-N-[1-(3-phenoxypropyl)-4-piperidyl]-2H-1,4-benzoxazine-8-carboxamide hydrochlorideHCID 19871153—

반응 단계

A solution of 2.3 g of 6-chloro-3,4-dihydro-3-oxo-2H-1,4-benzoxazine-8-carboxylic acid in 100 ml of tetrahydrofuran is cooled to below 0° C. and 2 ml of triethylamine is added under stirring thereto. Further, 1.1 g of ethyl chlorocarbonate is added and the mixture is stirred for 3 hours. To the resultant mixture is added 2.5 g of 4-amino-1-(3-phenoxypropyl)piperidine and the mixture stirred for 8 hours followed by collecting by filtration and washing with tetrahydrofuran and water. To a suspension of thus obtained crystals in 100 ml of methanol are added 10 ml of 10% hydrochloric acid and 30 ml of water and then the suspension is stirred. The collection of the crystals by filtration gives 6-chloro-3,4-dihydro-3-oxo-N-[1-(3-phenoxypropyl)-4-piperidyl]-2H-1,4 -benzoxazine-8-carboxamide hydrochloride, melting at 290°-300° C. with decomposition.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04892872
출처 데이터셋uspto-grants-1990_01
ORD IDord-fb1a7cbae0144f33855a560d2893804c
출처 메모uspto-grants-1990_01