돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 5826생성일: 2026년 10월 24일

Oxalic Acid → 4-(N-allyl-N-methylaminoacetyl)-2-(4-chlorophenyl)-3,4-dihydro-2H-1,4-benzothiazine oxalate

https://huagongshe.com/ko/reaction/5826

반응식

참여 물질

역할이름HCID투입량
반응물Oxalic AcidHCID 971—
반응물Allyl bromideHCID 7841—
반응물Potassium CarbonateHCID 11430—
반응물2-(4-chlorophenyl)-4-(N-methylaminoacetyl)-3,4-dihydro-2H-1,4-benzothiazineHCID 18984435—
용매WaterHCID 962—
용매Diethyl EtherHCID 3283—
용매DimethylformamideHCID 6228—
생성물4-(N-allyl-N-methylaminoacetyl)-2-(4-chlorophenyl)-3,4-dihydro-2H-1,4-benzothiazine oxalateHCID 18984433—

반응 단계

A mixture of 2-(4-chlorophenyl)-4-(N-methylaminoacetyl)-3,4-dihydro-2H-1,4-benzothiazine (1.80 g), allyl bromide (0.52 ml), potassium carbonate (2.25 g) and dimethylformamide (20 ml) is stirred at room temperature for 3.5 hours. The reaction mixture is poured into water, and the mixture is extracted with ethyl acetate. After the solvent is distilled off, the residue is purified by silica gel column chromatography (solvent, chloroform:methanol=40:1). The caramel thus obtained is dissolved in ether and thereto is added 1.1 equivalent of oxalic acid. The resulting precipitate is washed with ether and dried to give 4-(N-allyl-N-methylaminoacetyl)-2-(4-chlorophenyl)-3,4-dihydro-2H-1,4-benzothiazine oxalate as powder.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05246929
출처 데이터셋uspto-grants-1993_09
ORD IDord-95b2bc44ff6d4a949fc4fdaff92f4f93
출처 메모uspto-grants-1993_09