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

Trifluoroacetic acid → 2-(6-Methoxy-1,3,4,9-tetrahydro-beta-carboline-2-sulfonylmethyl)-3-methylbutyric acid

HRID 1582040
노트
인쇄 미리보기

반응식

HRID 1582040 반응식
FC(F)(F)C(O)=O.C([O:12][C:13](=[O:37])[CH:14]([CH2:18][S:19]([N:22]1[CH2:34][CH2:33][C:32]2[C:31]3[C:26](=[CH:27][CH:28]=[C:29]([O:35][CH3:36])[CH:30]=3)[NH:25][C:24]=2[CH2:23]1)(=[O:21])=[O:20])[CH:15]([CH3:17])[CH3:16])(C)(C)C.ClCCl.CO>ClCCl>[CH3:36][O:35][C:29]1[CH:30]=[C:31]2[C:26](=[CH:27][CH:28]=1)[NH:25][C:24]1[CH2:23][N:22]([S:19]([CH2:18][CH:14]([CH:15]([CH3:17])[CH3:16])[C:13]([OH:37])=[O:12])(=[O:21])=[O:20])[CH2:34][CH2:33][C:32]2=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6422Trifluoroacetic acidHCID 21226129Dichloromethane methanolHCID 698956642-(6-Methoxy-1,3,4,9-tetrahydro-beta-carboline-2-sulfonylmethyl)-3-methylbutyric acid tert-butyl ester

생성물 1

HCID 101778142-(6-Methoxy-1,3,4,9-tetrahydro-beta-carboline-2-sulfonylmethyl)-3-methylbutyric acid수율 62%

시약·촉매·용매 1

HCID 6344
Dichloromethane
용매

실험 절차

Trifluoroacetic acid (1 ml) was added to a solution of 2-(6-methoxy-1,3,4,9-tetrahydro-β-carboline-2-sulfonylmethyl)-3-methyl-butyric acid tert-butyl ester (237 mg) in dichloromethane (10 ml) at room temperature under nitrogen. The mixture was stirred for 2 h before being evaporated under reduced pressure. The residue was partitioned between 1M aqueous sodium hydroxide (15 ml) and diethyl ether (15 ml). The organics were extracted with 1M aqueous sodium hydroxide (15 ml). The combined aqueous portions were acidified to pH=5 with 10% citric acid and extracted with ethyl acetate (4×20 ml). The combined organics were washed with water (2×10 ml) and brine (10 ml), then dried (MgSO4), filtered and the solvent removed under reduced pressure to give, after chromatography (SiO2, 20:1 dichloromethane-methanol), the title compound (128 mg, 62%) as a white foam.

후처리

  1. custombefore being evaporated under reduced pressure
  2. customThe residue was partitioned between 1M aqueous sodium hydroxide (15 ml) and diethyl ether (15 ml)
  3. extractionThe organics were extracted with 1M aqueous sodium hydroxide (15 ml)
  4. extractionextracted with ethyl acetate (4×20 ml)
  5. washThe combined organics were washed with water (2×10 ml) and brine (10 ml)
  6. dry with materialdried (MgSO4)
  7. filtrationfiltered
  8. customthe solvent removed under reduced pressure
  9. customto give

출처 및 근거

ORD 기록
ord-e6dcdd1abf2e40f1a7d64572afb839b3
출처 데이터셋
uspto-grants-2004_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06734189B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트