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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 347900생성일: 2026년 10월 24일

Ammonia → HCID 178457107, 화합물

https://huagongshe.com/ko/reaction/347900

반응식

참여 물질

역할이름HCID투입량
반응물AmmoniaHCID 222—
반응물PropylamineHCID 7852—
반응물1,1,1-Trimethoxy-2-chloroethaneHCID 144702—
반응물2-(Chloromethyl)-1,3-benzoxazoleHCID 2061989—
반응물9-AminominocyclineHCID 54676112—
반응물n-Propylaminomethyl benzoxazoleHCID 60677375—
용매DimethylformamideHCID 6228—
생성물HCID 178457107HCID 178457107—

반응 단계

9-aminominocycline sulfate salt (1.0 g, 1.50 mmol) is dissolved in DMF (50 mL) and treated with a solution of 2-chloro-1,1,1-trimethoxyethane (0.463 g, 3.00 mmol, 2 equivalents). The reaction is stirred at room temperature until mass spectrometry shows conversion to the chloromethylbenzoxazole derivative. The solution is then treated with n-propylamine (10 mL, excess) and stirred until mass spectrometry shows conversion to the n-propylaminomethyl benzoxazole. The mixture is concentrated under reduced pressure to remove excess n-propylamine, and then poured slowly into ether (1 L) and HCl/ether is added to precipate the salt. The solid is rinsed with fresh ether and dried under vacuum. The crude solid is dissolved in water (100 mL) giving a solution at pH 2. The pH is raised successively by 0.5 units with aqueous ammonia, and extracted with dichloromethane. The fractions extracted at pH 4–4.5 are combined, dried (Na2SO4), filtered and concentrated nearly to dryness. A small volume of methanol is added and the solution is treated with 1M HCl in ether. The precipitated solid is collected by filtration, washed with fresh ether and dried under vacuum to yield 0.067 g of the product as its HCl salt.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07176225B2
출처 데이터셋uspto-grants-2007_02
ORD IDord-4335d33fec944396a3c54b10160f8090
출처 메모uspto-grants-2007_02