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Rademacher, P., Science of Synthesis, (2009) 40, 1175.
In an analogous way to ureas (see Section 40.7.1.1.11), N-alkylsulfamides 142 react with hypochlorite in basic solution to afford mono-, 1,1-, and 1,2-dialkylhydrazines 143 (Scheme 66).[158,159]
Meeeee 88 Meee- eee Meeeeeeeeeeee Meeeeeeeee eeee M-Meeeeeeeeeeeeee[888,888]
M8 | M8 | M8 | Meeeeeeeee | Meeee (%) | Mee |
---|---|---|---|---|---|
Me | M | M | 8 M MeMM, MeMMe (8 eeeee), 8 eee | 88 | [888] |
Me | M | M | 8 M MeMM, MeMMe (8 eeeee), 8 eee | 88 | [888] |
Me | Me | M | 8 M MeMM, MeMMe (8 eeeee), 8–8°M | 88 | [888] |
Me | Me | M | 8 M MeMM, MeMMe (8 eeeee), 8–8°M | 88 | [888] |
Me | M | Me | 8 M MeMM, MeMMe (8 eeeee), 88°M | 88 | [888] |
eMe | M | eMe | 8 M MeMM, MeMMe (8 eeeee) | 88 | [888] |
eMe | M | eMe | 8 M MeMM, MeMMe (8 eeeee), 88°M | 88 | [888] |
e-Me | M | e-Me | 8. MeM, eeeeeee, ee, 8 e 8. e-MeMMe, eeeeeee, −88°M, 8 e 8. ee, 8 e |
88 | [888] |
Meeeeeeeeeee Meeeeeeee
Meeeeeeeeeeeee (888, M8 = Me; M8 = M8 = M); Meeeeee Meeeeeeee:[888]
M eeee ee M-eeeeeeeeeeeeee (888, M8 = Me; M8 = M8 = M; 8.88 e, 8.88 eeee) ee 8 M MeMM eee eeeeeee eeee 88% MeMMe eeee (8.88 eM, 8.88 eeee). Mee eeeeeeeee eeeeeee eee eeee ee ee 8 eee. Meeee eeeeeeeeeeeee eeee eee ee MMe eee eeeeeee ee eeeeeee, MeMMM8 eee eeeee ee ee eeeeeee ee eee eeee eee eee eeeee eee eeeeeeeeee ee eeeeeeeeee eeeeeeeee; eeeee: 8.88 e (88%).
References
[158] | Meee, M.; Meeeeeeeee, M., Meeeee Meeeeee Mee. Meee., (8888) 888, 88. |
[159] | Meeee, M.-M.; Meeeeeeee, M., M. Meee. Mee., Meeeee Meeee. 8, (8888), 8888. |
Meeeeee Meeeeeeeeee
- 8.Meeeee-Meee, (8888) M 88-8, 8888.
- 8.Meeeee-Meee, (8888) M 88-8, 8888.
- 8.Meeeee-Meee, (8888) M 88e8, 888.
- 8.Meeeee-Meee, (8888) M 88e8, 888.