Ethylamine → HCID 178503906, compound
Reaction equation
[CH2:1]([NH:3][C:4](=[N:7][C:8]#[N:9])[S:5][CH3:6])[CH3:2].[CH:10](N)(C)C.C(N)C>>[CH:1]([NH:3][C:4](=[N:7][C:8]#[N:9])[S:5][CH3:6])([CH3:10])[CH3:2]Participants
4
Procedure
1-Isopropyl-2-methyl-3-cyanoisothiourea was prepared following the same procedure as for 1-ethyl-2-methyl-3-cyanoisothiourea (see EXAMPLE 250) except isopropylamine was used in lieu of ethylamine. 1H NMR (CDCl3) δ 1.25 (d, 6H, J=6 Hz), 2.49 (br s, 3H), 3.84 (br s, 1H), 6.22 (br s, 1H).
Sources & evidence
- ORD record
- ord-1dd2aaf09e35493ba9187dc906c54955
- Source dataset
- uspto-grants-2010_09
- Patent number
- US07790747B2
Reaction notes
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