Potassium Phosphate, Tribasic → HCID 178513786, compound

HRID 2428044Notes

Reaction equation

HRID 2428044 reaction equation
[NH2:1][C:2]1[C:3]([C:30]([O:32]CC)=O)=[N:4][C:5]([C:23]2[CH:28]=[CH:27][CH:26]=[C:25]([OH:29])[CH:24]=2)=[N:6][C:7]=1[NH:8][C@H:9]1[CH2:14][CH2:13][C@H:12]([NH:15]C(OC(C)(C)C)=O)[CH2:11][CH2:10]1.[NH2:35]C1C(C(OCC)=O)=NC(Cl)=NC=1N[C@H]1CC[C@H](NC(OC(C)(C)C)=O)CC1.[OH:63][C:64]1C=C(B(O)O)C=CC=1.C1(P(C2CCCCC2)C2C=CC=CC=2C2C(OC)=CC=CC=2OC)CCCCC1.P([O-])([O-])([O-])=O.[K+].[K+].[K+]>O1CCCC1.C([O-])(=O)C.[Pd+2].C([O-])(=O)C.O>[NH2:15][C@H:12]1[CH2:13][CH2:14][C@H:9]([N:8]2[C:64](=[O:63])[NH:1][C:2]3[C:7]2=[N:6][C:5]([C:23]2[CH:28]=[CH:27][CH:26]=[C:25]([OH:29])[CH:24]=2)=[N:4][C:3]=3[C:30]([NH2:35])=[O:32])[CH2:10][CH2:11]1

Participants

9

Procedure

Ethyl 5-amino-6-(trans-4-(tert-butoxycarbonylamino)cyclohexylamino)-2-(3-hydroxyphenyl)pyrimidine-4-carboxylate. Ethyl 5-amino-6-(trans-4-(tert-butoxycarbonylamino)cyclohexylamino)-2-chloropyrimidine-4-carboxylate. (0.500 g, 1.21 mmol), 3-hydroxyphenylboronic acid (0.249 g, 1.81 mmol), dicyclohexyl(2′,6′-dimethoxybiphenyl-2-yl)phosphine (0.075 g, 0.182 mmol), palladium acetate (0.041 g, 0.182 mmol) and potassium phosphate (0.52 g, 2.42 mmol) were combined in tetrahydrofuran (7 mL) and water (0.6 mL) and heated to 120° C. in a Biotage Emrys Optimizer microwave reactor for thirty min. The reaction solution was filtered and concentrated. The residue purified via Biotage chromatography (0 to 60% ethyl acetate in hexanes) to afford the title compound (0.150 g, 26%). MS (ESI) m/z 472[M+1]+.

Workup

  1. filtrationThe reaction solution was filtered
  2. concentrationconcentrated
  3. customThe residue purified via Biotage chromatography (0 to 60% ethyl acetate in hexanes)

Sources & evidence

ORD record
ord-f558f09a965d4078b63ed0e537fcb700
Source dataset
uspto-grants-2011_06
Patent number
US07968556B2

Reaction notes

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