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Carbon Disulfide → (10aS)-1,5,10,10a-Tetrahydro-3H-[1,3]thiazolo[3,4-b]isoquinoline-3-thione

HRID 461807
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HRID 461807 반응식
[C:1](=[S:3])=[S:2].OS(O[CH2:9][C@@H:10]1[CH2:19][C:18]2[C:13](=[CH:14][CH:15]=[CH:16][CH:17]=2)[CH2:12][NH:11]1)(=O)=O>[OH-].[Na+]>[CH2:9]1[C@H:10]2[N:11]([CH2:12][C:13]3[CH:14]=[CH:15][CH:16]=[CH:17][C:18]=3[CH2:19]2)[C:1](=[S:3])[S:2]1
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참가 물질

4

반응물 2

HCID 6348Carbon DisulfideHCID 54239900(S)-3-hydroxysulphonyloxymethyl1,2,3,4-tetrahydroisoquinoline

생성물 1

HCID 54272298(10aS)-1,5,10,10a-Tetrahydro-3H-[1,3]thiazolo[3,4-b]isoquinoline-3-thione수율 84.6%

시약·촉매·용매 1

HCID 14798Sodium Hydroxide용매

실험 절차

Carbon disulphide (40 g.) is added dropwise at 20° C., with vigorous stirring, to a solution of (S)-3-hydroxysulphonyloxymethyl-1,2,3,4-tetrahydroisoquinoline (100 g) in 0.25N sodium hydroxide solution (4,000 cc.). The reaction is exothermic. A solid precipitates and the reaction mixture then sets solid. Stirring is continued for 3 hours. The reaction mixture is neutralised by adding 4N hydrochloride acid. The crystals formed are filtered off, washed copiously with water and then recrystallised from ethanol (3,000 cc.) to give (S)-1,5,10,10a-tetrahydrothiazolo[3,4-b]-isoquinoline-3-thione (77 g. ) in the form of fine white needles melting at 150° C.

후처리

  1. customA solid precipitates
  2. additionby adding 4N hydrochloride acid
  3. customThe crystals formed
  4. filtrationare filtered off
  5. washwashed copiously with water
  6. customrecrystallised from ethanol (3,000 cc.)

출처 및 근거

ORD 기록
ord-557bfc469eee41c7a30337231207ac01
출처 데이터셋
uspto-grants-1977_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04064247

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