홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

p-Toluenesulfonic acid monohydrate → (3S)-3-Fluoropyrrolidine 4-methylbenzenesulfonate

HRID 494300
노트
인쇄 미리보기

반응식

HRID 494300 반응식
O.[CH3:2][C:3]1[CH:8]=[CH:7][C:6]([S:9]([OH:12])(=[O:11])=[O:10])=[CH:5][CH:4]=1.C([N:20]1[CH2:24][CH2:23][C@H:22]([F:25])[CH2:21]1)(OC(C)(C)C)=O>C(#N)C>[CH3:2][C:3]1[CH:4]=[CH:5][C:6]([S:9]([OH:12])(=[O:11])=[O:10])=[CH:7][CH:8]=1.[F:25][C@H:22]1[CH2:23][CH2:24][NH:20][CH2:21]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 521998p-Toluenesulfonic acid monohydrateHCID 18453464tert-Butyl (3S)-3-fluoropyrrolidine-1-carboxylate

생성물 1

HCID 86614633(3S)-3-Fluoropyrrolidine 4-methylbenzenesulfonate

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

4-Methylbenzenesulfonic acid monohydrate (752 mg, 3.95 mmol) was added to a stirred solution of Step 2 intermediate (280 mg, 1.48 mmol) in dry acetonitrile (20 ml) and the mixture was stirred at room temperature for 24 h under nitrogen atmosphere. The solvent was evaporated under reduced pressure and the oily residue obtained was triturated with dry diethyl ether (10 ml) to give 563 mg of the product as a white crystalline solid, which was used as such for the next step; IR (neat) 3443, 3019, 2783, 1626, 1434, 1215, 1034 cm−1

후처리

  1. customThe solvent was evaporated under reduced pressure
  2. customthe oily residue obtained
  3. customwas triturated with dry diethyl ether (10 ml)

출처 및 근거

ORD 기록
ord-a5d751681e0c4ae9808204ba7622b34a
출처 데이터셋
uspto-grants-2009_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07538128B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트