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Trimethyl orthoformate → N-(4-{[(1-methyl-1H-imidazol-2-ylmethyl)-(1-trityl-1H-imidazol-2-ylmethyl)-amino]-methyl}-benzyl)-N',N'-dipropyl-butane-1,4-diamine

HRID 2080887
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HRID 2080887 반응식
[CH3:1][N:2]1[CH:6]=[CH:5][N:4]=[C:3]1[CH2:7][N:8]([CH2:34][C:35]1[CH:42]=[CH:41][C:38]([CH:39]=O)=[CH:37][CH:36]=1)[CH2:9][C:10]1[N:11]([C:15]([C:28]2[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=2)([C:22]2[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=2)[C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=2)[CH:12]=[CH:13][N:14]=1.C(OC)(OC)OC.[CH2:50]([N:53]([CH2:59][CH2:60][CH3:61])[CH2:54][CH2:55][CH2:56][CH2:57][NH2:58])[CH2:51][CH3:52].[BH4-].[Na+]>CO.O>[CH3:1][N:2]1[CH:6]=[CH:5][N:4]=[C:3]1[CH2:7][N:8]([CH2:34][C:35]1[CH:42]=[CH:41][C:38]([CH2:39][NH:58][CH2:57][CH2:56][CH2:55][CH2:54][N:53]([CH2:59][CH2:60][CH3:61])[CH2:50][CH2:51][CH3:52])=[CH:37][CH:36]=1)[CH2:9][C:10]1[N:11]([C:15]([C:28]2[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=2)([C:22]2[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=2)[C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=2)[CH:12]=[CH:13][N:14]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 9005Trimethyl orthoformateHCID 4311764Sodium borohydrideHCID 7138396N,N-dipropylbutane-1,4-diamineHCID 866149174-{[(1-methyl-1H-imidazol-2-ylmethyl)-(1-trityl-1H-imidazol-2-ylmethyl)-amino]-methyl}-benzaldehyde

생성물 1

HCID 67103810N-(4-{[(1-methyl-1H-imidazol-2-ylmethyl)-(1-trityl-1H-imidazol-2-ylmethyl)-amino]-methyl}-benzyl)-N',N'-dipropyl-butane-1,4-diamine
수율 85.4%

시약·촉매·용매 2

HCID 887Methanol용매2회HCID 962Water용매

실험 절차

The compound (47.2 mg) obtained in Example 91-1 was dissolved in methanol (1.0 ml) and trimethyl orthoformate (28.0 μl) and a methanol solution containing the compound (14.7 mg) obtained in Example 1-2 were dropped thereto at room temperature under a nitrogen atmosphere. The whole was stirred for 12 hours. Sodium borohydride (10.0 mg) was added thereto under ice-cooling and the whole was warmed back to room temperature and stirred for 2 hours. After completion of the reaction, water was added thereto. The solvent was distilled off under reduced pressure. The resultant was diluted with chloroform and added with water, and the aqueous layer was subjected to extraction with chloroform. The combined organic layer was washed with a saturated saline solution and dried with anhydrous sodium sulfate. After filtration, the solution was concentrated and evaporated to dryness under reduced pressure and the residue was purified through silica gel column chromatography (chloroform/methanol), thereby obtaining the subject compound (51.6 mg) as a pale-yellow solid.

후처리

  1. additionwere dropped
  2. customat room temperature
  3. temperatureunder ice-cooling
  4. stirringstirred for 2 hours
  5. additionwas added
  6. distillationThe solvent was distilled off under reduced pressure
  7. additionThe resultant was diluted with chloroform
  8. additionadded with water
  9. extractionthe aqueous layer was subjected to extraction with chloroform
  10. washThe combined organic layer was washed with a saturated saline solution
  11. dry with materialdried with anhydrous sodium sulfate
  12. filtrationAfter filtration
  13. concentrationthe solution was concentrated
  14. customevaporated to dryness under reduced pressure
  15. customthe residue was purified through silica gel column chromatography (chloroform/methanol)

출처 및 근거

ORD 기록
ord-2dfc476cc08843c79f51972aaace6af0
출처 데이터셋
uspto-grants-2011_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07932281B2

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