Acetic Anhydride → HCID 178476679, compound

HRID 1087528Notes

Reaction equation

HRID 1087528 reaction equation
OC[C:3]1[CH:4]=[C:5]([C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)[C:6](=[O:16])[N:7]2[C:12]=1[C:11]1[S:13][CH:14]=[CH:15][C:10]=1[CH2:9][CH2:8]2.[C:23]([O:26][C:27](=O)C)(=[O:25])[CH3:24]>N1C=CC=CC=1>[C:23]([O:26][CH2:27][SH:13]1[C:11]2[C:12]3[N:7]([CH2:8][CH2:9][C:10]=2[CH:15]=[CH:14]1)[C:6](=[O:16])[C:5]([C:17]1[CH:18]=[CH:19][CH:20]=[CH:21][CH:22]=1)=[CH:4][CH:3]=3)(=[O:25])[CH3:24]

Participants

4

Reactant 2

HCID 7918Acetic AnhydrideHCID 14666699HCID 14666699, compound

Product 1

HCID 178476679HCID 178476679, compound

Reagents, catalysts & solvents 1

HCID 1049PyridineSolvent

Procedure

A suspension of 1.55 g of 4,5-dihydro-10-(hydroxymethyl)-8-phenyl-7H-thieno[2.3-a]quinolizin-7-one in 6.7 ml of pyridine was treated with 3.35 ml of acetic anhydride while stirring, whereby a clear solution was obtained after about 15 minutes. After stirring overnight, the precipitated yellow crystals were removed by filtration under suction and washed with ether. The filtrate was evaporated in vacuo and the residue together with the above yellow crystals were recrystallized from methanol. There was obtained pure (4,5-dihydro-7-oxo-8-phenyl-thieno[2,3-a]-quinolizin-1-yl)methyl acetate of m.p. 145°-146°.

Workup

  1. customwhereby a clear solution was obtained after about 15 minutes
  2. stirringAfter stirring overnight
  3. customthe precipitated yellow crystals were removed by filtration under suction
  4. washwashed with ether
  5. customThe filtrate was evaporated in vacuo
  6. customthe residue together with the above yellow crystals were recrystallized from methanol

Sources & evidence

ORD record
ord-e334bc5834d943cf9b23c65af73eee38
Source dataset
uspto-grants-1991_07
Patent number
US05036066

Reaction notes

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