HCID 178479678, compound → HCID 178519703, compound

HRID 2295351Notes

Reaction equation

HRID 2295351 reaction equation
Cl.[O:2]1[CH:6]=[CH:5][CH:4]=[C:3]1[C:7]([N:9]1[C:14]2[CH:15]=[CH:16][N:17]=[CH:18][C:13]=2[NH:12][C:11]([C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)=[N:10]1)=[O:8]>C(N(CC)CC)C>[O:2]1[CH:6]=[CH:5][CH:4]=[C:3]1[C:7]([N:9]1[C:14]2[CH:15]=[CH:16][N:17]=[CH:18][C:13]=2[NH:12][C:11]([C:19]2[CH:20]=[CH:21][CH:22]=[CH:23][CH:24]=2)=[N:10]1)=[O:8]

Participants

3

Reactant 1

HCID 178479678HCID 178479678, compound

Product 1

HCID 178519703HCID 178519703, compoundYield 95%

Reagents, catalysts & solvents 1

HCID 8471TriethylamineSolvent

Procedure

1-Furoyl-3-phenyl-1,4-dihydropyrido[3,4-e]-as-triazine hydrochloride, prepared as described in Example 8, is treated with an ethanolic solution of triethyl amine to obtain 1-furoyl-3-phenyl-1,4-dihydropyrido[3,4-e]-as-triazine with a yield of 95%; m.p.: 202°-203° C.

Sources & evidence

ORD record
ord-d69758e19b584732a7dd959cf885adfd
Source dataset
uspto-grants-1984_01
Patent number
US04424351

Reaction notes

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