Cyanamide → HCID 12272866, compound
Reaction equation
Cl.[C:2]([CH2:4][C:5](=[NH:10])[O:6][CH:7]([CH3:9])[CH3:8])#[N:3].[N:11]#[C:12]N>>[C:12]([N:10]=[C:5]([O:6][CH:7]([CH3:9])[CH3:8])[CH2:4][C:2]#[N:3])#[N:11]Participants
3
Procedure
3.25 g of isopropyl cyanoacetimidate hydrochloride and 1.26 g of cyanamide were treated with the same manner as in Example 1 and 2.07 g of isopropyl N-cyanocyanoacetimidate was obtained (yield 68.5%) mp 66.5°C. Analysis calculated for C7H9N3O (%) C 55.62, H 6.00, N 27.80, found C 55.41, H 5.91, N 27.66.
Sources & evidence
- ORD record
- ord-564f53be905e40ae8806af7e6a0e1887
- Source dataset
- uspto-grants-1976_04
- Patent number
- US03948915
Reaction notes
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