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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Hydrochloric Acid → HCID 10542363, 화합물

HRID 21580
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HRID 21580 반응식
[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:9](=[CH:10][CH:11]=1)[NH:8][C:7]([C:12]([O:14][CH3:15])=[O:13])=[CH:6]2.[CH3:16][S:17]([CH3:19])=O.[ClH:20]>CO>[Cl-:20].[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:9](=[CH:10][CH:11]=1)[NH:8][C:7]([C:12]([O:14][CH3:15])=[O:13])=[C:6]2[S+:17]([CH3:19])[CH3:16]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 313Hydrochloric Acid3회HCID 679Dimethyl SulfoxideHCID 27281841H-Indole-2-carboxylic acid, 5-methoxy-, methyl ester

생성물 1

HCID 10542363HCID 10542363, 화합물수율 52%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

A mixture of methyl 5-methoxy-1H-indole-2-carboxylate (8.3 g, 40 mmol; Blaikie KG, Perkin WH Jr, J. Chem. Soc. 1924;125:296) and dimethyl sulfoxide (4.0 mL, 4.4 g, 56 mmol) in 75 mL of methanol is cooled in ice and treated with gaseous HCl. The temperature of the reaction mixture increases to 45° C. as the HCl is added. Additional HCl is added intermittently and the rate of cooling is adjusted so that a reaction temperature of 40°-50° C. is maintained for 3 hours. The mixture is cooled and the precipitated solid filtered and washed with ether to yield 6.3 g (52%) of [5-methoxy-2-(methoxycarbonyl)-1H-indol-3-yl] dimethylsulfonium chloride suitable for further synthesis; mp 130° C.-dec.

후처리

  1. temperatureis cooled in ice
  2. additionis added
  3. temperaturethe rate of cooling
  4. customis adjusted so that a reaction temperature of 40°-50° C.
  5. temperatureis maintained for 3 hours
  6. temperatureThe mixture is cooled
  7. filtrationthe precipitated solid filtered
  8. washwashed with ether

출처 및 근거

ORD 기록
ord-6f015bcee68545a8a8caebae396ee2f2
출처 데이터셋
uspto-grants-1995_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05424329

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