Ethyl Acetate → HCID 22257954, compound

HRID 1611028Notes

Reaction equation

HRID 1611028 reaction equation
Cl[C:2]1[CH:3]=[C:4]([CH:9]=C[CH:11]=1)[C:5](OO)=[O:6].[OH:12][C:13]1[CH:14]=[C:15]([S:19]([C:21]2[C:29]3[C:28](=[O:30])[N:27]([CH3:31])[C:26](=[O:32])[N:25]([CH2:33][CH:34]([CH3:36])[CH3:35])[C:24]=3[S:23][C:22]=2[CH2:37][C:38]2[C:47]3[C:42](=[CH:43][CH:44]=[CH:45][CH:46]=3)[CH:41]=[CH:40][CH:39]=2)=[O:20])[CH:16]=[CH:17][CH:18]=1.C(OCC)(=O)C>ClCCl>[CH3:11][CH2:2][CH2:3][CH:4]([CH3:9])[CH3:5].[OH:12][C:13]1[CH:14]=[C:15]([S:19]([C:21]2[C:29]3[C:28](=[O:30])[N:27]([CH3:31])[C:26](=[O:32])[N:25]([CH2:33][CH:34]([CH3:35])[CH3:36])[C:24]=3[S:23][C:22]=2[CH2:37][C:38]2[C:47]3[C:42](=[CH:43][CH:44]=[CH:45][CH:46]=3)[CH:41]=[CH:40][CH:39]=2)(=[O:6])=[O:20])[CH:16]=[CH:17][CH:18]=1

Participants

6

Procedure

3-Chloroperoxybenzoic acid (50 mg) was added to a solution of 5-[(3-hydroxyphenyl)sulfinyl]-3-methyl-1-(2-methylpropyl)-6-(1-naphthalenylmethyl)thieno[2,3-d]pyrimidine-2,4-(1H,3H)-dione (Example 28, 80 mg) in dichloromethane (2 ml). After 2 hours, ethyl acetate (25 ml) was added and the solution was washed with saturated sodium bisulfite solution (10 ml), then with saturated sodium hydrogen carbonate solution (10 ml), then with brine (10 ml). The organic layer was dried over anhydrous magnesium sulfate, filtered and evaporated under reduced pressure. The residue was recrystallised from ethyl acetate:isohexane to give the title compound (24 mg).

Workup

  1. washthe solution was washed with saturated sodium bisulfite solution (10 ml)
  2. dry with materialThe organic layer was dried over anhydrous magnesium sulfate
  3. filtrationfiltered
  4. customevaporated under reduced pressure
  5. customThe residue was recrystallised from ethyl acetate

Sources & evidence

ORD record
ord-9d1e6958c0e94ca88f481b79504879da
Source dataset
uspto-grants-2006_01
Patent number
US06984644B2

Reaction notes

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