HCID 67199810, compound → HCID 86621654, compound

HRID 1711382Notes

Reaction equation

HRID 1711382 reaction equation
[ClH:1].[NH2:2][C:3]1[N:8]=[C:7]([NH:9][C:10]2[CH:15]=[CH:14][C:13]([NH:16]C(=O)C)=[CH:12][CH:11]=2)[CH:6]=[C:5]([CH3:20])[N:4]=1>Cl>[ClH:1].[NH2:16][C:13]1[CH:12]=[CH:11][C:10]([NH:9][C:7]2[CH:6]=[C:5]([CH3:20])[N:4]=[C:3]([NH2:2])[N:8]=2)=[CH:15][CH:14]=1

Participants

3

Procedure

To a suspension of 16 (6.0 g, 20 mmol) was added 2N HCl (40 mL) and the mixture was refluxed for 20 h. The solvents were evaporated to dryness, residue boiled in MeOH and diluted with EtOAc. The resulting precipitate was filtered and washed with EtOAc and dried to give essentially pure 17 (5.0 g, 97%); mp (MeOH/EtOAc) 275-280° C.; 1H NMR [(CD3)2SO] δ 12.50 (br, 1H, N+H), 10.75 (br s, 1H, NH), 9.75 (br s, 2H, NH2), 7.85 (br s, 4H, NH2 & ArH)), 7.34 (d, J=8.6 Hz, 2H, ArH), 6.24 (br s, 1H, ArH), 2.79 (s, 3H, CH3), HRMS (FAB+) calc. for C11H14N5 (M+1) m/z 216.1249, found 216.1247.

Workup

  1. temperaturethe mixture was refluxed for 20 h
  2. customThe solvents were evaporated to dryness, residue
  3. additiondiluted with EtOAc
  4. filtrationThe resulting precipitate was filtered
  5. washwashed with EtOAc
  6. customdried

Sources & evidence

ORD record
ord-ee4cb32609a14141abd2a69cdf555849
Source dataset
uspto-grants-2010_09
Patent number
US07790746B2

Reaction notes

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