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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2395828생성일: 2026년 10월 24일

Hydrochloric Acid → Hydrochloric Acid

https://huagongshe.com/ko/reaction/2395828

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물SufentanilHCID 41693—
반응물Propionyl chlorideHCID 62324—
반응물4-(Methoxymethyl)-N-phenyl-1-[2-(2-thienyl)ethyl]-4-piperidinamineHCID 15295498—
용매Diethyl EtherHCID 3283—
용매DichloromethaneHCID 6344—
용매TriethylamineHCID 8471—
생성물Hydrochloric AcidHCID 313—
생성물164790-60-7HCID 18463211—

반응 단계

Propionyl chloride (1.3 equivalents) was added to a 0.4M methylene chloride solution of 6 in a glass stoppered RB flask at RT. A mild exotherm developed and analysis by LC at the end of 40 minutes showed 90% sufentanil 7 with about 7% starting material 6. About 8% by weight of triethylamine was then added and stirred for another 40 minutes at RT. LC showed 95% product with no trace of starting material 6. The mixture was then quenched with an excess of dilute ammonium hydroxide and the lower methylene chloride layer was separated, washed with water and dried. Evaporation of methylene chloride gave a yellow powder which by LC amounted to 95% sufentanil 7. This was converted to HCl salt by dissolving in ether (250 ml) and stirring with 4N HCl [100 ml]. The precipitated HCl salt was filtered off, washed with ether and air-dried. Recrystallization from water (6 ml for every gm of Sufentanil.HCl) gave sufentanil HCl (19.6 g) as white paste with LC purity of 99.50%. The isolated yield of the pure HCl salt was 85%. H1NMR (CDCl3): δ7.25-6.85 (m,8H), 4.05 (s,2H), 3.35 (s,3H), 3.14-1.56 (m,14H), 0.95 (t,3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05489689
출처 데이터셋uspto-grants-1996_02
ORD IDord-94076dbe99b148209ca5db418832a78b
출처 메모uspto-grants-1996_02