Dimethyl Sulfoxide → 2-chloro-6a,7,9,10-tetrahydro-[1,4]oxazino[3,4-h]pteridin-6(5H)-one

HRID 2386213Notes

Reaction equation

HRID 2386213 reaction equation
[Cl:1][C:2]1[N:7]=[C:6](Cl)[C:5]([NH2:9])=[CH:4][N:3]=1.CCN(C(C)C)C(C)C.[NH:19]1[CH2:24][CH2:23][O:22][CH2:21][CH:20]1[C:25](O)=[O:26].CS(C)=O>O>[Cl:1][C:2]1[N:3]=[CH:4][C:5]2[NH:9][C:25](=[O:26])[CH:20]3[CH2:21][O:22][CH2:23][CH2:24][N:19]3[C:6]=2[N:7]=1

Participants

6

Conditions

Temperature
100 °C

Procedure

A round-bottomed flask equipped with a magnetic stirrer was added 2,4-dichloropyrimidin-5-amine (1.89 g, 11.52 mmol), DIPEA (8.05 ml, 46.1 mmol), morpholine-3-carboxylic acid (1.66 g, 12.68 mmol), and DMSO (5 ml). The reaction was stirred at 100° C. overnight. The reaction mixture was poured into water and extracted with EtOAc 3 times. The pH of the aqueous layer was adjusted (about 5) with 10% citric acid and extracted again with EtOAc. The combined organic layer dried over MgSO4, filtered, and concentrated in vacuo to furnish a tan solid. The solid was triturated in diethyl ether containing a small amount of EtOH, filtered, and dried to give 2-chloro-6a,7,9,10-tetrahydro-[1,4]oxazino[3,4-h]pteridin-6(5H)-one: 1.95 g (70.3%). MS [M+H] found 241.

Workup

  1. customA round-bottomed flask equipped with a magnetic stirrer
  2. extractionextracted with EtOAc 3 times
  3. extractionextracted again with EtOAc
  4. dry with materialThe combined organic layer dried over MgSO4
  5. filtrationfiltered
  6. concentrationconcentrated in vacuo
  7. customto furnish a tan solid
  8. customThe solid was triturated in diethyl ether containing a small amount of EtOH
  9. filtrationfiltered
  10. customdried

Sources & evidence

ORD record
ord-277134972fb4446f9dd25a25a73ed72a
Source dataset
uspto-grants-2012_09
Patent number
US08268819B2

Reaction notes

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