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Hydrochloric Acid → Dibenzo[b,f][1,4]thiazepine-11(10H)-thione

HRID 1082064
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HRID 1082064 반응식
P12(SP3(SP(SP(S3)(S1)=S)(=S)S2)=S)=[S:2].[CH:15]1[C:20]2[C:21](=O)[NH:22][C:23]3[CH:29]=[CH:28][CH:27]=[CH:26][C:24]=3[S:25][C:19]=2[CH:18]=[CH:17][CH:16]=1.Cl>N1C=CC=CC=1>[CH:15]1[C:20]2[C:21](=[S:2])[NH:22][C:23]3[CH:29]=[CH:28][CH:27]=[CH:26][C:24]=3[S:25][C:19]=2[CH:18]=[CH:17][CH:16]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 14817Phosphorus sulfide (P2S5)HCID 374829Dibenzothiazepinone

생성물 1

HCID 667552Dibenzo[b,f][1,4]thiazepine-11(10H)-thione

시약·촉매·용매 1

HCID 1049Pyridine용매

실험 절차

Phosphorus pentasulphide (1.2 eq) was added to a solution of 10,11-dihydrodibenzo[b,f][1,4]thiazepin-11-one (1.14 g, 5 mmol) in pyridine (40 ml) and heated under reflux for 15 hr. The mixture was allowed to cool and poured into hydrochloric acid (1.3M) at 0° C. Filtration of the yellow precipitate and purification by chromatography on silica (eluting with dichloromethane/methanol, 99:1) followed by recrystallisation from ethanol gave the title compound as yellow crystals (700 mg, m.p. 245°-246° C., Rf 0.81, CH2Cl2/MeOH9:1).

후처리

  1. temperatureheated
  2. temperatureunder reflux for 15 hr
  3. temperatureto cool
  4. filtrationFiltration of the yellow precipitate and purification by chromatography on silica (eluting with dichloromethane/methanol, 99:1)
  5. customfollowed by recrystallisation from ethanol

출처 및 근거

ORD 기록
ord-98462676614b4174ba429cf321c63b5c
출처 데이터셋
uspto-grants-1996_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05589474

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