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Toluene → HCID 67215620, compound

HRID 1677565
Notes
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Reaction equation

HRID 1677565 reaction equation
C([N:3](CC)CC)C.C1(P(N=[N+]=[N-])(C2C=CC=CC=2)=O)C=CC=CC=1.[CH3:25][O:26][C:27]([C:29]1[CH:30]=[C:31]([CH:46]=[CH:47][C:48]=1[N+:49]([O-:51])=[O:50])[C:32]([C:34]1[N:38]2[CH:39]=[C:40](C(O)=O)[CH:41]=[CH:42][C:37]2=[CH:36][N:35]=1)=[O:33])=[O:28].[C:52](=[O:55])(O)[O-:53].[Na+].[C:57]1([CH3:63])[CH:62]=CC=C[CH:58]=1>O.C(O)(C)(C)C>[C:57]([O:53][C:52]([NH:3][C:40]1[CH:41]=[CH:42][C:37]2[N:38]([C:34]([C:32]([C:31]3[CH:46]=[CH:47][C:48]([N+:49]([O-:51])=[O:50])=[C:29]([CH:30]=3)[C:27]([O:26][CH3:25])=[O:28])=[O:33])=[N:35][CH:36]=2)[CH:39]=1)=[O:55])([CH3:63])([CH3:62])[CH3:58]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

8

Reactant 5

HCID 1140TolueneHCID 8471TriethylamineHCID 199401P,P-Diphenylphosphinic azideHCID 516892Sodium BicarbonateHCID 67215444HCID 67215444, compound

Product 1

HCID 67215620HCID 67215620, compound

Reagents, catalysts & solvents 2

HCID 962WaterSolventHCID 6386tert-ButanolSolvent

Conditions

Temperature
110 °C

Procedure

0.55 ml (3.96 mmol) of triethylamine and 1.07 ml of tertbutanol, followed by 0.31 ml (1.40 mmol) of diphenylphosphoryl azide, are added to 430 mg (1.16 mmol) of 3-[3-(methoxycarbonyl)-4-nitrobenzoyl]imidazo[1,5-a]pyridine-6-carboxylic acid in 20 ml of toluene. The reaction medium is heated at 110° C. for 3 hours and then cooled to ambient temperature. Water and a saturated aqueous sodium bicarbonate solution are added and then the extraction is carried out with ethyl acetate. The organic phase is separated by settling, washed with a saturated aqueous sodium chloride solution, then dried over sodium sulfate and concentrated under reduced pressure. The product is purified by column chromatography on silica gel, elution being carried out with a mixture of dichloromethane and methanol (98/2). 480 mg of an orange-colored solid are obtained. Melting point: 182° C.; 1H NMR (d6-DMSO): 1.55 (9H, s), 3.92 (3H, s), 7.45 (1H, d), 7.90 (1H, s), 7.99 (1H, d), 8.24 (1H, d), 8.67 (1H, d), 8.76 (1H, s), 9.89 (1H, s)

Workup

  1. temperaturecooled to ambient temperature
  2. extractionthe extraction
  3. customThe organic phase is separated
  4. washwashed with a saturated aqueous sodium chloride solution
  5. dry with materialdried over sodium sulfate
  6. concentrationconcentrated under reduced pressure
  7. customThe product is purified by column chromatography on silica gel, elution
  8. additionbeing carried out with a mixture of dichloromethane and methanol (98/2)

Sources & evidence

ORD record
ord-05e218e305da4931ae7f30f4046c007f
Source dataset
uspto-grants-2011_08
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08008321B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes