Potassium Phosphate, Tribasic → HCID 59752684, compound

HRID 749735Notes

Reaction equation

HRID 749735 reaction equation
C(OC([N:8]1[CH2:17][CH2:16][C:15]2[N:14]([CH2:18][C:19]3[CH:24]=[CH:23][C:22]([Cl:25])=[CH:21][CH:20]=3)[N:13]=[C:12]([C:26]3[CH:31]=[CH:30][C:29]([Cl:32])=[CH:28][CH:27]=3)[C:11]=2[CH2:10][CH2:9]1)=O)(C)(C)C.C(OC(N1CCC2N(CC3C=CC(Cl)=CC=3)N=C(S(C(F)(F)F)(=O)=O)C=2CC1)=O)(C)(C)C.[O-]P([O-])([O-])=O.[K+].[K+].[K+].ClC1C=CC(B(O)O)=CC=1>C1COCC1>[Cl:25][C:22]1[CH:21]=[CH:20][C:19]([CH2:18][N:14]2[C:15]3[CH2:16][CH2:17][NH:8][CH2:9][CH2:10][C:11]=3[C:12]([C:26]3[CH:31]=[CH:30][C:29]([Cl:32])=[CH:28][CH:27]=3)=[N:13]2)=[CH:24][CH:23]=1

Participants

6

Procedure

1-(4-Chloro-benzyl)-3-(4-chloro-phenyl)-4,5,7,8-tetrahydro-1H-1,2,6-triaza-azulene-6-carboxylic acid tert-butyl ester. To a solution of 142.7 mg of 1-(4-chloro-benzyl)-3-trifluoromethanesulfonyl-4,5,7,8-tetrahydro-1H-1,2,6-triaza-azulene-6-carboxylic acid tert-butyl ester, prepared as in Example 43, Steps A through C, in 3 mL of THF was added 0.17 g of K3PO4, 54.9 mg of 4-chlorophenylboronic acid, and 22.1 mg of PdCl2dppf. The mixture was heated at reflux for 48 h. The mixture was filtered through diatomaceous earth, rinsing with toluene, and the filtrate was concentrated in vacuo. Chromatography on SiO2 (hexanes to 75% EtOAc/hexanes) afforded 6.7 mg of the desired compound. MS (ESI): exact mass calculated for C25H27Cl2N3O2, 471.15; found, m/z 472.1 [M+H]+.

Workup

  1. temperatureThe mixture was heated
  2. temperatureat reflux for 48 h
  3. filtrationThe mixture was filtered through diatomaceous earth
  4. washrinsing with toluene
  5. concentrationthe filtrate was concentrated in vacuo

Sources & evidence

ORD record
ord-93fc4d530cd94efd81991815e02e3289
Source dataset
uspto-grants-2008_07
Patent number
US07402680B2

Reaction notes

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