Ethyl 5-furan-2-yl-4-oxo-3,4-dihydrothieno[2,3-d]pyrimidine-2-carboxylate → HCID 178522984, compound

HRID 606387Notes

Reaction equation

HRID 606387 reaction equation
O=C1C2C(=CC=CC=2)N=C(C(OCC)=O)N1.[O:17]1[CH:21]=[CH:20][CH:19]=[C:18]1[C:22]1[C:30]2[C:29](=[O:31])[NH:28][C:27]([C:32]([O:34]CC)=O)=[N:26][C:25]=2[S:24][CH:23]=1.C1(C(C2C=CC=CC=2)(C2C=CC=CC=2)N2C=NC(CCCOC3C=C(CN)C=CN=3)=N2)C=CC=CC=1.C1(C(C2C=CC=CC=2)(C2C=CC=CC=2)[N:80]2[CH:84]=[N:83][C:82]([O:85][CH2:86][CH2:87][O:88][C:89]3[CH:90]=[C:91]([CH2:95][NH2:96])[CH:92]=[CH:93][CH:94]=3)=[N:81]2)C=CC=CC=1>>[O:17]1[CH:21]=[CH:20][CH:19]=[C:18]1[C:22]1[C:30]2[C:29](=[O:31])[NH:28][C:27]([C:32]([NH:96][CH2:95][C:91]3[CH:92]=[CH:93][CH:94]=[C:89]([O:88][CH2:87][CH2:86][O:85][C:82]4[N:83]=[CH:84][NH:80][N:81]=4)[CH:90]=3)=[O:34])=[N:26][C:25]=2[S:24][CH:23]=1

Participants

5

Reactant 4

HCID 59298719Ethyl 5-furan-2-yl-4-oxo-3,4-dihydrothieno[2,3-d]pyrimidine-2-carboxylateHCID 667687691-[2-({3-[1-(triphenylmethyl)-1H-1,2,4-triazol-3-yl]propyl}oxy)pyridin-4-yl]methanamineHCID 667690991-{3-[(2-([1-(triphenylmethyl)-1H-1,2,4-triazol-3-yl]oxy)ethyl)oxy}phenyl]methanamineHCID 135437466Ethyl 4-oxo-3,4-dihydroquinazoline-2-carboxylate

Product 1

HCID 178522984HCID 178522984, compound

Procedure

By a method similar to that in Example 22, and using, instead of ethyl 4-oxo-3,4-dihydro-2-quinazolinecarboxylate, ethyl 5-furan-2-yl-4-oxo-3,4-dihydrothieno[2,3-d]pyrimidine-2-carboxylate obtained in Reference Example 40 and using, instead of 1-[2-({3-[1-(triphenylmethyl)-1H-1,2,4-triazol-3-yl]propyl}oxy)pyridin-4-yl]methaneamine, 1-{3-[(2-{[1-(triphenylmethyl)-1H-1,2,4-triazol-3-yl]oxy}ethyl)oxy]phenyl}methanamine obtained in Reference Example 32, the title compound was obtained as a white powder (23.0 mg, 7%).

Workup

  1. customobtained in Reference Example 40
  2. customobtained in Reference Example 32

Sources & evidence

ORD record
ord-bc0dcf61b7f04d89a87cf162dbe24612
Source dataset
uspto-grants-2011_03
Patent number
US07915267B2

Reaction notes

Loading…