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Hydrochloric Acid → HCID 13825032, 화합물

HRID 713189
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반응식

HRID 713189 반응식
[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[S:8]([CH:11]1[CH2:16][CH2:15][N:14](C(OC(C)(C)C)=O)[CH2:13][CH2:12]1)(=[O:10])=[O:9].Cl>O1CCOCC1>[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[S:8]([CH:11]1[CH2:16][CH2:15][NH:14][CH2:13][CH2:12]1)(=[O:9])=[O:10]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 118159133HCID 118159133, 화합물

생성물 1

HCID 13825032HCID 13825032, 화합물

시약·촉매·용매 1

HCID 312751,4-Dioxane용매2회

실험 절차

A solution of tert-butyl 4-((2-fluorophenyl)sulfonyl)piperidine-1-carboxylate (1.31 g, 3.82 mmol) in dioxane (12.7 mL) at room temperature was treated with 4M HCl in dioxane (9.55 ml, 38.2 mmol). The reaction mixture was allowed to stir at room temperature overnight. The reaction mixture was concentrated under reduced pressure. The resulting white solid was triturated with hexanes, filtered, collected, and lyophilized overnight to give the title compound, as its HCl salt, as a white solid (815.1 mg, 76%). ESI-MS m/z [M+H]+243.95.

후처리

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
  1. concentrationThe reaction mixture was concentrated under reduced pressure
  2. customThe resulting white solid was triturated with hexanes
  3. filtrationfiltered
  4. customcollected
  5. waitlyophilized overnight

출처 및 근거

ORD 기록
ord-e784ccd5cc964131a76013787026fc16
출처 데이터셋
uspto-grants-2015_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09181249B2

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