Potassium Phosphate, Tribasic → HCID 57474587, compound

HRID 391626Notes

Reaction equation

HRID 391626 reaction equation
[NH2:1][C:2]1[C:3]([C:20]([O-:22])=O)=[N:4][C:5]([C:13]2[CH:18]=[CH:17][CH:16]=[C:15]([OH:19])[CH:14]=2)=[N:6][C:7]=1[NH:8][C:9]([CH3:12])([CH3:11])[CH3:10].[NH2:23]C1C(C([O-])=O)=NC(Cl)=NC=1NC(C)(C)C.[OH:39][C:40]1C=C(B(O)O)C=CC=1.P([O-])([O-])([O-])=O.[K+].[K+].[K+].C1(P(C2CCCCC2)C2C=CC=CC=2C2C(OC)=CC=CC=2OC)CCCCC1>O1CCCC1.O.C([O-])(=O)C.[Pd+2].C([O-])(=O)C>[C:9]([N:8]1[C:40](=[O:39])[NH:1][C:2]2[C:7]1=[N:6][C:5]([C:13]1[CH:18]=[CH:17][CH:16]=[C:15]([OH:19])[CH:14]=1)=[N:4][C:3]=2[C:20]([NH2:23])=[O:22])([CH3:11])([CH3:10])[CH3:12]

Participants

9

Procedure

5-Amino-6-tert-butylamino-2-(3-hydroxy-phenyl)-pyrimidine-4-carboxylate. In a microwave flask was placed 5-amino-6-tert-butylamino-2-chloro-pyrimidine-4-carboxylate (0.46 g, 1.69 mmol), 3-hydroxyphenylboronic acid (0.35 g, 2.53 mmol), potassium phosphate (0.72 g, 3.4 mmol), dicyclohexyl(2′,6′-dimethoxybiphenyl-2-yl)phosphine (0.10 g, 0.25 mmol) and palladium (II) acetate (0.06 g, 0.25 mmol) in tetrahydrofuran (17 mL) and water (1.7 mL). The mixture was reacted according to General Procedure E. The crude residue was purified using Biotage silica gel chromatography (0-35% ethyl acetate in hexanes) to afford the title compound (0.26 g, 0.79 mmol, 36% yield). MS (ESI) m/z 331.4 [M+1]+.

Workup

  1. customIn a microwave flask was placed
  2. customThe mixture was reacted
  3. customThe crude residue was purified

Sources & evidence

ORD record
ord-3ac64303d88a4add865f4c2e93bc9928
Source dataset
uspto-grants-2013_02
Patent number
US08383634B2

Reaction notes

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