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Formaldehyde → 3-(3,5-Dichloro-4-methoxybenzoyl)-5-trifluoromethyl-2,3-dihydro-1,3-benzothiazole

HRID 385161
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인쇄 미리보기

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HRID 385161 반응식
Cl.NC1C=C(C(F)(F)F)C=CC=1S.[F:14][C:15]([F:26])([F:25])[C:16]1[CH:17]=[CH:18][C:19]2[S:23][CH2:22][NH:21][C:20]=2[CH:24]=1.C=O.[Cl:29][C:30]1[CH:31]=[C:32]([CH:36]=[C:37]([Cl:41])[C:38]=1[O:39][CH3:40])[C:33](Cl)=[O:34]>ClCCl.O.C(N(CC)CC)C>[Cl:29][C:30]1[CH:31]=[C:32]([CH:36]=[C:37]([Cl:41])[C:38]=1[O:39][CH3:40])[C:33]([N:21]1[C:20]2[CH:24]=[C:16]([C:15]([F:14])([F:25])[F:26])[CH:17]=[CH:18][C:19]=2[S:23][CH2:22]1)=[O:34]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

8

반응물 4

HCID 712FormaldehydeHCID 27346782-Amino-4-(trifluoromethyl)benzenethiol hydrochlorideHCID 38303153,5-Dichloro-4-methoxybenzoyl chlorideHCID 218361675-Trifluoromethyl-2,3-dihydro-1,3-benzothiazole

생성물 1

HCID 681090693-(3,5-Dichloro-4-methoxybenzoyl)-5-trifluoromethyl-2,3-dihydro-1,3-benzothiazole

시약·촉매·용매 3

HCID 962
Water
용매
HCID 6344Dichloromethane용매
HCID 8471Triethylamine용매2회

실험 절차

2-amino-4-trifluoromethylbenzenethiol hydrochloride (502 mg), and 5-trifluoromethyl-2,3-dihydro-1,3-benzothiazole synthesized from 37% formalin (0.18 mL) and triethylamine (0.30 mL) in the same manner as in Example 38 were dissolved in dichloromethane (5 mL), and triethylamine (0.30 mL) and 3,5-dichloro-4-methoxybenzoyl chloride (354 mg) were added to the solution, and then the mixture was stirred at room temperature for 2 hours. Water was added and the mixture was extracted with ethyl acetate. The organic layer was washed with 1N hydrochloric acid, 1N sodium hydroxide and saturated brine, and then dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure and the obtained residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=8:1) to obtain the title compound (223 mg) as a colorless oily substance.

후처리

  1. extractionthe mixture was extracted with ethyl acetate
  2. washThe organic layer was washed with 1N hydrochloric acid, 1N sodium hydroxide and saturated brine
  3. dry with materialdried over anhydrous sodium sulfate
  4. distillationThe solvent was distilled off under reduced pressure
  5. customthe obtained residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=8:1)

출처 및 근거

ORD 기록
ord-d5012945561b40dab83d8844f581d420
출처 데이터셋
uspto-grants-2013_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08367843B2

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