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m-Chloroperbenzoic acid → 4-Acetyl-6-chloro-2,3,4,5-tetrahydro-1,4-benzothiazepine 1-oxide

HRID 1079325
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HRID 1079325 반응식
ClC1C=CC=C(C(OO)=[O:9])C=1.[C:12]([N:15]1[CH2:21][C:20]2[C:22]([Cl:26])=[CH:23][CH:24]=[CH:25][C:19]=2[S:18][CH2:17][CH2:16]1)(=[O:14])[CH3:13]>ClCCl>[C:12]([N:15]1[CH2:21][C:20]2[C:22]([Cl:26])=[CH:23][CH:24]=[CH:25][C:19]=2[S:18](=[O:9])[CH2:17][CH2:16]1)(=[O:14])[CH3:13]
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참가 물질

4

반응물 2

HCID 70297m-Chloroperbenzoic acidHCID 98376804-Acetyl-6-chloro-2,3,4,5-tetrahydro-1,4-benzothiazepine

생성물 1

HCID 102207644-Acetyl-6-chloro-2,3,4,5-tetrahydro-1,4-benzothiazepine 1-oxide

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

실험 절차

A solution of 3-chloroperbenzoic acid (1.14 g) in dichloromethane (100 ml) was added dropwise with cooling from 0° C. to -2° C. to a stirred solution of 4-acetyl-6-chloro-2,3,4,5-tetrahydro-1,4-benzothiazepine (1.34 g, prepared as Example 9 above) in dichloromethane (50 ml). The reaction mixture was stirred for 15 minutes, washed with water, dried and the solvent was removed by evaporation at reduced pressure. Purification of the residue by flash chromatography using dichloromethane/ethanol (95:5) as eluent gave 4-acetyl-6-chloro-2,3,4,5-tetrahydro-1,4-benzothiazepine 1-oxide, which was recrystallised from ethyl acetate. Yield 1.15 g (m.p. 119°-121° C.).

후처리

  1. washwashed with water
  2. customdried
  3. customthe solvent was removed by evaporation at reduced pressure
  4. customPurification of the residue by flash chromatography

출처 및 근거

ORD 기록
ord-3c268fbe2ed54558a799f9b25e0286dd
출처 데이터셋
uspto-grants-1996_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05580866

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