Carbonochloridic acid, 4-methoxyphenyl ester → HCID 53889674, compound
Reaction equation
[CH3:1][O:2][N:3]=[C:4]([C:7]1[CH2:8][NH:9][CH2:10][CH2:11][CH:12]=1)[C:5]#[N:6].[CH3:13][O:14][C:15]1[CH:20]=[CH:19][C:18]([O:21][C:22](Cl)=[O:23])=[CH:17][CH:16]=1>>[CH3:1][O:2][N:3]=[C:4]([C:7]1[CH2:8][N:9]([C:22]([O:21][C:18]2[CH:19]=[CH:20][C:15]([O:14][CH3:13])=[CH:16][CH:17]=2)=[O:23])[CH2:10][CH2:11][CH:12]=1)[C:5]#[N:6]Participants
3
Procedure
α-(Methoxyimino)-α-(1,2,5,6-tetrahydropyridin-3-yl)acetonitrile (D8) (0.5 g, 0.003 moles) was treated with 4-methoxyphenylchloroformate (0.5 ml, 0.0033 moles) as in the method of Example 1. The crude produce was triturated with pentane to give the title compound (E4) as a white crystalline solid (0.81 g, 85%) m.p. 75°-76° C.
Workup
- customThe crude produce
- customwas triturated with pentane
Sources & evidence
- ORD record
- ord-8e25a8e0387c4f4a887c6c7d99864b87
- Source dataset
- uspto-grants-1994_10
- Patent number
- US05356914
Reaction notes
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