Thionyl Chloride → HCID 178499502, compound

HRID 2422161Notes

Reaction equation

HRID 2422161 reaction equation
Cl.[N+:2]([C:5]1[CH:10]=[CH:9][C:8]([CH2:11][C:12](=[NH:14])[NH2:13])=[CH:7][CH:6]=1)([O-:4])=[O:3].[C:15]([CH:18]([CH2:23][C:24]([O:26][CH3:27])=[O:25])[C:19](OC)=[O:20])(=O)[CH3:16].C[O-].[Na+].S(Cl)(Cl)=O>CO.CC(C)=O>[CH3:27][O:26][C:24](=[O:25])[CH2:23][C:18]1[C:19]([OH:20])=[N:14][C:12]([CH2:11][C:8]2[CH:7]=[CH:6][C:5]([N+:2]([O-:4])=[O:3])=[CH:10][CH:9]=2)=[N:13][C:15]=1[CH3:16]

Participants

7

Procedure

A mixture of 2-(4-nitrophenyl)ethanimidamide hydrochloride (0.22 g, 1.0 mmol), dimethyl acetyl-succinate (0.19 g, 1.0 mmol), and sodium methoxide (0.07 g, 1.3 mmol) in MeOH (10 mL) was refluxed for 15 hours. After cooling to room temperature, the separated solids were collected by suction and added to a pre-formed solution of thionyl chloride (0.65 mL, 8.9 mmol) in MeOH (7.5 mL). The resulting mixture was refluxed for 16 hours and then cooled to room temperature. Acetone was added and the precipitated solids were collected by suction, rinsed with acetone and dried under high vacuum for 4 hours to give methyl[4-hydroxy-6-methyl-2-(4-nitrobenzyl)-pyrimidin-5-yl]acetate (0.12 g, 38% yield) as a white solid.

Workup

  1. temperaturewas refluxed for 15 hours
  2. customthe separated solids were collected by suction
  3. temperatureThe resulting mixture was refluxed for 16 hours
  4. temperaturecooled to room temperature
  5. customthe precipitated solids were collected by suction
  6. washrinsed with acetone
  7. customdried under high vacuum for 4 hours

Sources & evidence

ORD record
ord-abdff7696dd64a149d9640dd05486a9e
Source dataset
uspto-grants-2011_06
Patent number
US07960393B2

Reaction notes

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