Ethyl isocyanate → HCID 66746737, compound
Reaction equation
[Cl-].[C:2]([C:4]1[C:16]([N+:17]([O-])=O)=[CH:15][CH:14]=[CH:13][C:5]=1[O:6][CH2:7][C@@H:8]1[CH2:12][CH2:11][CH2:10][NH2+:9]1)#[N:3].[CH2:20]([N:22]=[C:23]=[O:24])[CH3:21]>>[NH2:17][C:16]1[C:4]([C:2]#[N:3])=[C:5]([CH:13]=[CH:14][CH:15]=1)[O:6][CH2:7][C@@H:8]1[CH2:12][CH2:11][CH2:10][N:9]1[C:23]([NH:22][CH2:20][CH3:21])=[O:24]Participants
3
Procedure
Prepared as in Example 191a from (S)-2-((2-cyano-3-nitrophenoxy)methyl)pyrrolidinium chloride (Example 191b) and ethyl isocyanate in 100% yield as a white solid. MS 289 (MH+).
Sources & evidence
- ORD record
- ord-38b4001b538c419b9274b423773c0b9e
- Source dataset
- uspto-grants-2015_04
- Patent number
- US09000054B2
Reaction notes
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