Propionyl chloride → HCID 66747087, compound
Reaction equation
Cl.[N+:2]([C:5]1[CH:12]=[CH:11][CH:10]=[C:9]([O:13][CH2:14][CH:15]2[CH2:19][CH2:18][NH:17][CH2:16]2)[C:6]=1[C:7]#[N:8])([O-:4])=[O:3].[C:20](Cl)(=[O:23])[CH2:21][CH3:22]>>[N+:2]([C:5]1[CH:12]=[CH:11][CH:10]=[C:9]([O:13][CH2:14][CH:15]2[CH2:19][CH2:18][N:17]([C:20](=[O:23])[CH2:21][CH3:22])[CH2:16]2)[C:6]=1[C:7]#[N:8])([O-:4])=[O:3]Participants
3
Procedure
Prepared as in Example 176b from 2-nitro-6-(pyrrolidin-3-ylmethoxy)benzonitrile hydrochloride (Example 196d) and propionyl chloride in 51% as a yellow solid. MS 304 (MH+).
Sources & evidence
- ORD record
- ord-845bb49b3abc40ffbbdcd93470ba1f8a
- Source dataset
- uspto-grants-2015_11
- Patent number
- US09181276B2
Reaction notes
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