7-amino-3,4-dihydro-2H-1,4-benzoxazin-3-one → HCID 69100202, compound

HRID 2115140Notes

Reaction equation

HRID 2115140 reaction equation
Cl[CH2:2][C:3]([N:5]1[CH2:10][CH2:9][CH:8]([CH2:11][C:12]2[CH:17]=[CH:16][C:15]([CH3:18])=[CH:14][CH:13]=2)[CH2:7][CH2:6]1)=[O:4].[NH2:19][C:20]1[CH:30]=[CH:29][C:23]2[NH:24][C:25](=[O:28])[CH2:26][O:27][C:22]=2[CH:21]=1>C(O)C>[CH3:18][C:15]1[CH:16]=[CH:17][C:12]([CH2:11][CH:8]2[CH2:9][CH2:10][N:5]([C:3](=[O:4])[CH2:2][NH:19][C:20]3[CH:30]=[CH:29][C:23]4[NH:24][C:25](=[O:28])[CH2:26][O:27][C:22]=4[CH:21]=3)[CH2:6][CH2:7]2)=[CH:13][CH:14]=1

Participants

4

Reactant 2

HCID 27641827-amino-3,4-dihydro-2H-1,4-benzoxazin-3-oneHCID 69100022HCID 69100022, compound

Product 1

HCID 69100202HCID 69100202, compound

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Procedure

The title compound is prepared from 2-chloro-1-[4-(4-methyl-benzyl)-piperidin-1-yl]-ethanone (Example 227a) and 7-amino-4H-benzo[1,4]oxazine-3-one according to the method described in Example 206. Melting Point: 206-208° C. (ethanol)

Sources & evidence

ORD record
ord-1bcd76dbe0bf468d884a14de051bd177
Source dataset
uspto-grants-2008_10
Patent number
US07435744B2

Reaction notes

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