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Dichloromethane → 1-(4-tert-Butylphenyl)homopiperazine dihydrochloride, 98%

HRID 511197
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반응식

HRID 511197 반응식
C(OC([N:8]1[CH2:14][CH2:13][CH2:12][N:11]([C:15]2[CH:20]=[CH:19][C:18]([C:21]([CH3:24])([CH3:23])[CH3:22])=[CH:17][CH:16]=2)[CH2:10][CH2:9]1)=O)(C)(C)C.FC(F)(F)C(O)=O.[Cl:32]CCl>>[ClH:32].[C:21]([C:18]1[CH:17]=[CH:16][C:15]([N:11]2[CH2:12][CH2:13][CH2:14][NH:8][CH2:9][CH2:10]2)=[CH:20][CH:19]=1)([CH3:24])([CH3:22])[CH3:23]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 6344DichloromethaneHCID 6422Trifluoroacetic acidHCID 58576748HCID 58576748, 화합물

생성물 1

HCID 666719201-(4-tert-Butylphenyl)homopiperazine dihydrochloride, 98%

실험 절차

To 4-(4-tert-butyl-phenyl)-[1,4]diazepane-1-carboxylic acid tert-butyl ester (541 mg; 16.3 mmol, prepared in accordance with Example 160) is added a 2:3 mixture of trifluoroacetic acid and dichloromethane (5 mL) and the resulting reaction mixture is stirred at room temperature for 2 hours. All volatiles are then removed under high vacuum and the residue is taken up in a 4 molar solution of hydrochloric acid in dioxane. The solution is allowed to stand over night and the precipitate formed is filtered, washed (diethyl ether) and dried under high vacuum to afford the desired compound (452 mg) which is used in the next step without further purification.

후처리

  1. customthe resulting reaction mixture
  2. customAll volatiles are then removed under high vacuum
  3. waitto stand over night
  4. customthe precipitate formed
  5. filtrationis filtered
  6. washwashed (diethyl ether)
  7. customdried under high vacuum

출처 및 근거

ORD 기록
ord-78a5da1781c54297b6ee8522cc4eb242
출처 데이터셋
uspto-grants-2015_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09096524B2

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