Formamide → 5,6-Dihydro-3H-pyrano[4',3':4,5]thieno[2,3-D]pyrimidin-4(8H)-one

HRID 1384861Notes

Reaction equation

HRID 1384861 reaction equation
C([O:3][C:4]([C:6]1[C:14]2[CH2:13][CH2:12][O:11][CH2:10][C:9]=2[S:8][C:7]=1[NH2:15])=O)C.[CH:16]([NH2:18])=O>>[N:15]1[C:7]2[S:8][C:9]3[CH2:10][O:11][CH2:12][CH2:13][C:14]=3[C:6]=2[C:4](=[O:3])[NH:18][CH:16]=1

Participants

3

Reactant 2

HCID 713FormamideHCID 10987982Ethyl 2-amino-5,7-dihydro-4H-thieno[2,3-c]pyran-3-carboxylate

Product 1

HCID 4032245,6-Dihydro-3H-pyrano[4',3':4,5]thieno[2,3-D]pyrimidin-4(8H)-oneYield 42%

Procedure

2-Amino-4,5-dihydro-7H-thieno[2,3-c]pyran-3-carboxylic acid ethyl ester (26 g, 0.114 mol) was dissolved in formamide (200 ml) and the resulting mixture was heated at reflux temperature for 1.5 h. After cooling to room temperature the precipitate was filtered off, washed with water (2×80 ml) and dried in vacuo at 50° C. for 18 h which afforded 10.0 g (42%) of 5,6-dihydro-8H-pyrano[4′,3′:4,5]thieno[2,3-d]pyrimidin-4-one as a solid.

Workup

  1. temperaturethe resulting mixture was heated
  2. temperatureat reflux temperature for 1.5 h
  3. filtrationwas filtered off
  4. washwashed with water (2×80 ml)
  5. customdried in vacuo at 50° C. for 18 h which

Sources & evidence

ORD record
ord-fe50e3e5647a4d24abed25001418e834
Source dataset
uspto-grants-2001_07
Patent number
US06262044B1

Reaction notes

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