Sodium Carbonate → HCID 178513290, compound

HRID 401073Notes

Reaction equation

HRID 401073 reaction equation
[O:1]=[C:2]1[NH:7][CH:6]([C:8]2[CH:9]=[C:10]([CH:13]=[CH:14][CH:15]=2)[C:11]#[N:12])[C:5]([C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=2)=[C:4]([C:22]2[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=2)[NH:3]1.[NH2:28][OH:29].Cl.C([O-])([O-])=O.[Na+].[Na+]>CO>[OH:29][NH:28][C:11](=[NH:12])[C:10]1[CH:13]=[CH:14][CH:15]=[C:8]([CH:6]2[C:5]([C:16]3[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=3)=[C:4]([C:22]3[CH:23]=[CH:24][CH:25]=[CH:26][CH:27]=3)[NH:3][C:2](=[O:1])[NH:7]2)[CH:9]=1

Participants

5

Reactant 3

HCID 10340Sodium CarbonateHCID 443297Hydroxyamine hydrochlorideHCID 67060962HCID 67060962, compound

Product 1

HCID 178513290HCID 178513290, compoundYield 19.5%

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Procedure

A mixture of 3-(2-oxo-5,6-diphenyl-1,2,3,4-tetrahydropyrimidin-4-yl)benzonitrile (700 mg, 2 mmol, 1 eq), NH2OH—HCl (144 mg, 2.2 mmol, 1.1 eq) and Na2CO3 (414 mg, 4.0 mmol, 2.0 eq) in methanol (5.0 mL) was heated to reflux overnight. The mixture was cooled to room temperature and filtered. The filtered mass was washed with methanol (5.0 mL) and purified by prep-HPLC to afford Compound 99 as a yellow solid (150 mg, 19.5%) and Compound 98 as a white solid (6.7%). Data for Compound 99: 1H NMR (MeOH-d4 500 MHz TMS): δ 7.69-7.72 (m, 2H), 7.58-7.61 (m, 2H), 7.26 (br, 5H), 7.04 (br, 2H), 6.88 (br, 2H), 5.51 (s 1H); MS (ESI): m/z 385.1.1 [M+1]+.

Workup

  1. temperaturewas heated
  2. temperatureto reflux overnight
  3. filtrationfiltered
  4. washThe filtered mass was washed with methanol (5.0 mL)
  5. custompurified by prep-HPLC

Sources & evidence

ORD record
ord-2a79c56429f848f79683481b38b914f3
Source dataset
uspto-grants-2014_06
Patent number
US08741915B2

Reaction notes

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