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Hydrochloric Acid → HCID 67589431, 화합물

HRID 863539
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HRID 863539 반응식
C([O:3][C:4](=[O:19])[CH2:5][C@H:6]1[CH2:18][CH2:17][N:9]2[C:10]3[C:15]([CH:16]=[C:8]2[CH2:7]1)=[CH:14][CH:13]=[CH:12][CH:11]=3)C.[OH-].[Na+].Cl>CO>[CH:14]1[CH:13]=[CH:12][CH:11]=[C:10]2[C:15]=1[CH:16]=[C:8]1[CH2:7][C@@H:6]([CH2:5][C:4]([OH:19])=[O:3])[CH2:18][CH2:17][N:9]12
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 86752148HCID 86752148, 화합물

생성물 1

HCID 67589431HCID 67589431, 화합물

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

A solution of 17 g (63 mmol) of methyl alpha (R or S)-ethyl-6,7,8,9-tetrahydropyrido[1,2-a]indole-8(S)-acetate (diastereomers A+B) in 150 ml of methanol was treated with 130 ml of 2M sodium hydroxide and heated to reflux for 18 hours. The cooled solution was added to 150 ml of 4M hydrochloric acid and the resulting precipitate was filtered off and partitioned between 200 ml of dichloromethane and 100 ml of water. The organic phase was separated, dried over magnesium sulfate and evaporated to give 15 g of alpha (R or S)-6,7,8,9-tetrahydropyrido[1,2-a]indole-8(S)-acetic acid (diastereomers A+B) as a pale pink solid.

후처리

  1. temperatureheated
  2. temperatureto reflux for 18 hours
  3. filtrationthe resulting precipitate was filtered off
  4. custompartitioned between 200 ml of dichloromethane and 100 ml of water
  5. customThe organic phase was separated
  6. dry with materialdried over magnesium sulfate
  7. customevaporated

출처 및 근거

ORD 기록
ord-84cf276662ae47a8ac27271807bbd30e
출처 데이터셋
uspto-grants-1998_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05721230

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