2-Bromoethanol → HCID 66833930, compound
Reaction equation
[OH:1][C:2]1[CH:3]=[CH:4][C:5]2[C:17](=[O:18])[C:16]3[C:15]4[C:10](=[CH:11][C:12]([C:19]#[N:20])=[CH:13][CH:14]=4)[NH:9][C:8]=3[C:7]([CH3:22])([CH3:21])[C:6]=2[CH:23]=1.[Br:24][CH2:25][CH2:26]O>>[Br:24][CH2:25][CH2:26][O:1][C:2]1[CH:3]=[CH:4][C:5]2[C:17](=[O:18])[C:16]3[C:15]4[C:10](=[CH:11][C:12]([C:19]#[N:20])=[CH:13][CH:14]=4)[NH:9][C:8]=3[C:7]([CH3:21])([CH3:22])[C:6]=2[CH:23]=1Participants
3
Procedure
Under the same conditions as the method for synthesizing Compound A7-1, the title compound was prepared from Compound A6 and 2-bromoethanol.
Workup
- customUnder the same conditions as the method for synthesizing Compound A7-1
Sources & evidence
- ORD record
- ord-92827526754f450aaf8cac94bb5dc63d
- Source dataset
- uspto-grants-2015_09
- Patent number
- US09126931B2
Reaction notes
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