Ethyl acetate hexane → HCID 67021312, compound
Reaction equation
[CH2:1]([O:3][C:4](=[O:21])[CH2:5][C:6]1[CH:11]=[CH:10][C:9]([NH:12][C:13]2[C:18]([NH2:19])=[CH:17][CH:16]=[CH:15][N:14]=2)=[CH:8][C:7]=1[Cl:20])[CH3:2].[CH3:22]CCCCC.CCOC(C)=O>>[CH2:1]([O:3][C:4](=[O:21])[CH2:5][C:6]1[CH:11]=[CH:10][C:9]([N:12]2[C:13]3=[N:14][CH:15]=[CH:16][CH:17]=[C:18]3[N:19]=[CH:22]2)=[CH:8][C:7]=1[Cl:20])[CH3:2]Participants
3
Procedure
The title compound is prepared as described in Step 1.2 but using [4-(3-amino-pyridin-2-ylamino)-2-chloro-phenyl]-acetic acid ethyl ester. Title compound: ES-MS: 316.1 [M+H]+; single peak at tR=4.24 min (System 1); Rf=0.16 (Hexane/EtOAc, 1:1).
Workup
- customThe title compound is prepared
Sources & evidence
- ORD record
- ord-569071fb039f42f49cfbf5b2a27d9952
- Source dataset
- uspto-grants-2011_10
- Patent number
- US08030311B2
Reaction notes
Loading…