Ethyl Acetate → HCID 57863142, compound

HRID 217139Notes

Reaction equation

HRID 217139 reaction equation
[N+:1]([C:4]1[CH:5]=[C:6]2[C:11](=[CH:12][CH:13]=1)[N:10]=[C:9]([C:14]1[CH:19]=[CH:18][C:17]3[O:20][CH2:21][O:22][C:16]=3[CH:15]=1)[N:8]=[CH:7]2)([O-:3])=[O:2].[CH3:23]COC(C)=O>>[N+:1]([C:4]1[CH:5]=[C:6]2[C:11](=[CH:12][CH:13]=1)[N:10]=[C:9]([C:14]1[CH:19]=[CH:18][C:17]3[O:20][CH2:21][CH2:23][O:22][C:16]=3[CH:15]=1)[N:8]=[CH:7]2)([O-:3])=[O:2]

Participants

3

Reactant 2

HCID 8857Ethyl AcetateHCID 578631566-Nitro-2-(1,3-benzodioxole-5-yl)-quinazoline

Product 1

HCID 57863142HCID 57863142, compoundYield 70%

Procedure

This compound was synthesized in 70% yield, according to the procedure described in example 3 for 6-nitro-2-(3,4-methylendioxy-phenyl)-quinazoline. C16H11N3O4, MW: 309.28; mp: 263-265; TLC (tol/AcOEt 7/3) Rf=0.80.

Workup

  1. customThis compound was synthesized in 70% yield

Sources & evidence

ORD record
ord-68a2b86c0b4b463c8791861249cecab1
Source dataset
uspto-grants-2012_06
Patent number
US08193353B2

Reaction notes

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