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Diisopropylethylamine → HCID 178418888, 화합물

HRID 7087
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HRID 7087 반응식
[C:1]([C:9]1[CH:19]=[CH:18][C:12]2[N:13]=[C:14]([CH2:16]Cl)[NH:15][C:11]=2[CH:10]=1)(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C(OC([N:27]([CH2:47][C:48]1[CH:53]=[CH:52][CH:51]=[CH:50][N:49]=1)[CH2:28][C:29]1[CH:34]=[CH:33][C:32]([CH2:35][NH:36][CH:37]2[C:46]3[N:45]=[CH:44][CH:43]=[CH:42][C:41]=3[CH2:40][CH2:39][CH2:38]2)=[CH:31][CH:30]=1)=O)(C)(C)C.C(N(CC)C(C)C)(C)C>CN(C=O)C>[N:49]1[CH:50]=[CH:51][CH:52]=[CH:53][C:48]=1[CH2:47][NH:27][CH2:28][C:29]1[CH:30]=[CH:31][C:32]([CH2:35][N:36]([CH2:16][C:14]2[NH:13][C:12]3[CH:18]=[CH:19][C:9]([C:1](=[O:8])[C:2]4[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=4)=[CH:10][C:11]=3[N:15]=2)[CH:37]2[C:46]3[N:45]=[CH:44][CH:43]=[CH:42][C:41]=3[CH2:40][CH2:39][CH2:38]2)=[CH:33][CH:34]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 81531DiisopropylethylamineHCID 1951252[2-(chloromethyl)-1H-benzimidazol-5-yl](phenyl)methanoneHCID 22018600N-(t-butoxycarbonyl)-N-(2-pyridinylmethyl)-N'-(5,6,7,8-tetrahydro-8-quinolinyl)-1,4-benzenedimethanamine

생성물 1

HCID 178418888HCID 178418888, 화합물수율 75.9%

시약·촉매·용매 1

HCID 6228Dimethylformamide
용매

실험 절차

A solution of 5-benzoyl-2-chloromethylbenzimidazole (284 mg, 1.05 mmol), N-(tert-butoxycarbonyl)-N-(2-pyridinylmethyl)-N′-(5,6,7,8-tetrahydro-8-quinolinyl)-1,4-benzenedimethanamine (476 mg, 1.04 mmol) and N,N-diisopropylethylamine (0.36 mL, 2.08 mmol) were stirred at 80□ C in DMF (4 mL) for 16 hours. The reaction was then cooled, concentrated under reduced pressure and diluted with CH2Cl2 (35 mL) and saturated aqueous NaHCO3 (40 mL). The phases were separated and the aqueous phase was washed with CH2Cl2 (2×25 mL). The combined organic extracts were washed with saturated aqueous NaHCO3 (1×40 mL), dried (NaSO4), filtered and concentrated under reduced pressure. Purification of the resultant oil by flash chromatography on silica gel (96:4 CH2Cl2/MeOH) provided the desired alkylated product (468 mg, 65%) as an orange oil.

후처리

  1. temperatureThe reaction was then cooled
  2. concentrationconcentrated under reduced pressure
  3. additiondiluted with CH2Cl2 (35 mL) and saturated aqueous NaHCO3 (40 mL)
  4. customThe phases were separated
  5. washthe aqueous phase was washed with CH2Cl2 (2×25 mL)
  6. washThe combined organic extracts were washed with saturated aqueous NaHCO3 (1×40 mL)
  7. dry with materialdried (NaSO4)
  8. filtrationfiltered
  9. concentrationconcentrated under reduced pressure
  10. customPurification of the resultant oil by flash chromatography on silica gel (96:4 CH2Cl2/MeOH)

출처 및 근거

ORD 기록
ord-c3e65d3523c4435f91103dac99cfb3aa
출처 데이터셋
uspto-grants-2006_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07084155B2

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