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1-Hydroxybenzotriazole → rac-N-(1-Azabicyclo[2.2.2]oct-3-yl)-5-nitro-1-benzothiophene-2-carboxamide hydrochloride

HRID 15452
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HRID 15452 반응식
CN(C([O:8][N:9]1N=N[C:11]2[CH:12]=[CH:13][CH:14]=[CH:15][C:10]1=2)=[N+](C)C)C.[B-](F)(F)(F)F.C1C=CC2N([OH:32])N=NC=2C=1.[ClH:33].Cl.[NH2:35][CH:36]1[CH:41]2[CH2:42][CH2:43][N:38]([CH2:39][CH2:40]2)[CH2:37]1.[N+](C1[S:51][C:50]([C:52](O)=[O:53])=[CH:49]C=1)([O-])=O.C(N(C(C)C)CC)(C)C>CN(C=O)C>[ClH:33].[N:38]12[CH2:43][CH2:42][CH:41]([CH2:40][CH2:39]1)[CH:36]([NH:35][C:52]([C:50]1[S:51][C:13]3[CH:12]=[CH:11][C:10]([N+:9]([O-:8])=[O:32])=[CH:15][C:14]=3[CH:49]=1)=[O:53])[CH2:37]2
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참가 물질

7

반응물 5

HCID 757711-HydroxybenzotriazoleHCID 805915-Nitro-2-thenoic acidHCID 81531DiisopropylethylamineHCID 197853Quinuclidine, 3-amino-, dihydrochlorideHCID 2733207O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate

생성물 1

HCID 10193833
rac-N-(1-Azabicyclo[2.2.2]oct-3-yl)-5-nitro-1-benzothiophene-2-carboxamide hydrochloride
수율 48.6%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

At RT, initially 244 mg (0.76 mmol) of TBTU and 104 mg (0.78 mmol) of HOBt followed by 153 mg (0.77 mmol) of 3-aminoquinuclidine dihydrochloride are added to a solution of 180 mg (0.81 mmol) of 5-nitrothiophene-2-carboxylic acid and diiso-propylethylamine (0.8 ml) in 4 ml of DMF. The mixture is stirred at RT for 4 h. For work-up, the mixture is concentrated and the residue is taken up in a mixture of chloroform and excess aqueous sodium hydroxide solution. The phases are separated and the aqueous phase is repeatedly re-extracted with chloroform. The combined organic phases are dried over sodium sulfate and concentrated, and the crude product is chromatographed on silica gel (mobile phase: chloroform/methanol/conc. ammonia 100:5:0.5→100:20:2). The resulting product is taken up in THF, excess HCl in diethyl ether is added, then the mixture is concentrated and the product is dried under high vacuum. 136 mg (47% of theory) of the hydrochloride are obtained.

후처리

  1. customAt RT
  2. concentrationFor work-up, the mixture is concentrated
  3. additionthe residue is taken up in a mixture of chloroform and excess aqueous sodium hydroxide solution
  4. customThe phases are separated
  5. extractionthe aqueous phase is repeatedly re-extracted with chloroform
  6. dry with materialThe combined organic phases are dried over sodium sulfate
  7. concentrationconcentrated
  8. customthe crude product is chromatographed on silica gel (mobile phase: chloroform/methanol/conc. ammonia 100:5:0.5→100:20:2)
  9. additionexcess HCl in diethyl ether is added
  10. concentrationthe mixture is concentrated
  11. customthe product is dried under high vacuum

출처 및 근거

ORD 기록
ord-f37e172f2ee944e69c1eea23992947aa
출처 데이터셋
uspto-grants-2010_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07732477B2

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