Ammonia methanol → 4-{[(1R)-1-(3-nitrophenyl)ethyl]amino}quinazoline-8-carboxamide

HRID 578654Notes

Reaction equation

[N+:1]([C:4]1[CH:5]=[C:6]([C@H:10]([NH:12][C:13]2[C:22]3[C:17](=[C:18]([C:23]([O:25]C)=O)[CH:19]=[CH:20][CH:21]=3)[N:16]=[CH:15][N:14]=2)[CH3:11])[CH:7]=[CH:8][CH:9]=1)([O-:3])=[O:2].[NH3:27].CO>>[N+:1]([C:4]1[CH:5]=[C:6]([C@H:10]([NH:12][C:13]2[C:22]3[C:17](=[C:18]([C:23]([NH2:27])=[O:25])[CH:19]=[CH:20][CH:21]=3)[N:16]=[CH:15][N:14]=2)[CH3:11])[CH:7]=[CH:8][CH:9]=1)([O-:3])=[O:2]

Participants

Reactant 2

HCID 21705897Ammonia methanol

HCID 66763746Methyl 4-{[(1R)-1-(3-nitrophenyl)ethyl]amino}quinazoline-8-carboxylate

Product 1

HCID 667629844-{[(1R)-1-(3-nitrophenyl)ethyl]amino}quinazoline-8-carboxamide

Procedure

A suspension of Methyl 4-{[(1R)-1-(3-nitrophenyl)ethyl]amino}quinazoline-8-carboxylate (7.26 g, 20.60 mmol) in 7 N ammonia/methanol (100 mL)

Sources & evidence

ORD record: ord-d1514dd1726b41b6989a7804cb601448
Source dataset: uspto-grants-2015_05
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US09040560B2

Reaction notes

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