Acetic Anhydride → HCID 13911281, compound

HRID 652254Notes

Reaction equation

HRID 652254 reaction equation
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=1[N:9]1[CH2:14][CH2:13][N:12]([CH2:15][CH2:16][N:17]2[C:22](=[O:23])[C:21]3[S:24][CH:25]=[CH:26][C:20]=3[NH:19][C:18]2=[O:27])[CH2:11][CH2:10]1.[C:28](OC(=O)C)(=[O:30])[CH3:29]>>[C:28]([N:19]1[C:20]2[CH:26]=[CH:25][S:24][C:21]=2[C:22](=[O:23])[N:17]([CH2:16][CH2:15][N:12]2[CH2:11][CH2:10][N:9]([C:4]3[CH:5]=[CH:6][CH:7]=[CH:8][C:3]=3[O:2][CH3:1])[CH2:14][CH2:13]2)[C:18]1=[O:27])(=[O:30])[CH3:29]

Participants

3

Reactant 2

HCID 7918Acetic AnhydrideHCID 139112783-[2-[4-(2-Methoxyphenyl)piperazin-1-yl]ethyl]thieno[3,2-d]pyrimidine-2,4-dione

Product 1

HCID 13911281HCID 13911281, compoundYield 57%

Procedure

A solution of 3-[2-[4-(2-methoxyphenyl)piperazin-1-yl]ethyl]thieno[3,2-d]pyrimidine-2,4-dione (2.6 g, 6.73 mmol) in acetic anhydride (30 ml) was heated to reflux for 5 hours. Acetic anhydride was removed in vacuo. The residue was dissolved in toluene, and the toluene was removed in vacuo. This process was repeated twice to remove any residual acetic anhydride. The residue was purified by flash chromatography on silica gel 60 (60 g) using 2.5% methanol in methylene chloride as eluant to give the product (1.65 g, 57% yield) as an off-white solid, mp 156°-158° C.

Workup

  1. temperatureto reflux for 5 hours
  2. customAcetic anhydride was removed in vacuo
  3. dissolutionThe residue was dissolved in toluene
  4. customthe toluene was removed in vacuo
  5. customto remove any residual acetic anhydride
  6. customThe residue was purified by flash chromatography on silica gel 60 (60 g)

Sources & evidence

ORD record
ord-2ba2cbf76a884237a9267958c4f078ff
Source dataset
uspto-grants-1987_06
Patent number
US04670560

Reaction notes

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