Aniline → HCID 15051732, compound

HRID 1723373Notes

Reaction equation

HRID 1723373 reaction equation
C(=O)(OCC1C2(O)ON(CC3C2N3)C2C1=C(O)C=C(C=O)C=2)N.NC1C=CC=CC=1.[C:31](=[O:59])([O:33][CH2:34][CH:35]1[C:47]2([OH:49])[O:48][N:42]([CH2:43][CH:44]3[CH:46]2[NH:45]3)[C:41]2[C:36]1=[C:37]([OH:58])[CH:38]=[C:39]([CH:50]=[N:51][C:52]1[CH:57]=[CH:56][CH:55]=[CH:54][CH:53]=1)[CH:40]=2)[NH2:32]>CO.[Pd]>[C:31](=[O:59])([O:33][CH2:34][CH:35]1[C:47]2([OH:49])[O:48][N:42]([CH2:43][CH:44]3[CH:46]2[NH:45]3)[C:41]2[C:36]1=[C:37]([OH:58])[CH:38]=[C:39]([CH2:50][NH:51][C:52]1[CH:53]=[CH:54][CH:55]=[CH:56][CH:57]=1)[CH:40]=2)[NH2:32]

Participants

6

Procedure

4-Formyl-6,9-dihydroxy-14-oxa-1,11-diazatetracyclo[7.4.1.02,7.010,12 ]tetradeca-2,4,6-trien-8-ylmethyl carbamate (50 mg) was dissolved in methanol (5 ml). Aniline (0.05 ml) was added to this solution and the mixture was allowed to stand at room temperature for 3 hours to give a solution containing 6,9-dihydroxy-4-phenyliminomethyl-14-oxa-1,11-diazatetracyclo[7.4.1.02,7.010,12 ]tetradeca-2,4,6-trien-8-ylmethyl carbamate. 10% Palladium on carbon (100 mg) was added to the solution, and the mixture was stirred for 2 hours at room temperature under hydrogen atmosphere (4.5 atm). The mixture was filtered through cellulose powder and the filter cake was washed with methanol (20 ml). The filtrate and the washings were combined and evaporated in vacuo. The residue was subjected to preparative thin layer chromatography, which was developed with a mixture of chloroform, methanol and water (65:25:4, v/v/v) to afford 4-anilinomethyl-6,9-dihydroxy-14-oxa-1,11-diazatetracyclo[7.4.1.02,7.010,12 ]tetradeca-2,4,6-trien-8-ylmethyl carbamate (25 mg).

Workup

  1. customto give a solution
  2. filtrationThe mixture was filtered through cellulose powder
  3. washthe filter cake was washed with methanol (20 ml)
  4. customevaporated in vacuo
  5. additionwas developed with a mixture of chloroform, methanol and water (65:25:4, v/v/v)

Sources & evidence

ORD record
ord-a3ab87b6c64341d9a39376a4101591d5
Source dataset
uspto-grants-1989_08
Patent number
US04861774

Reaction notes

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