Methylhydrazine → HCID 178481711, compound
Reaction equation
[CH3:1][NH:2][NH2:3].[Cl:4][C:5]1[CH:10]=[CH:9][C:8]([S:11]([N:14]2[CH:19]3[CH2:20][CH2:21][CH2:22][CH:15]2[CH:16]([C:24]([O:26]C)=O)[C:17](=O)[CH2:18]3)(=[O:13])=[O:12])=[CH:7][CH:6]=1.C(=O)(OC)OC.ClC1C=CC(S(N2C3CCCC2CC(=O)C3)(=O)=O)=CC=1>>[Cl:4][C:5]1[CH:10]=[CH:9][C:8]([S:11]([N:14]2[CH:19]3[CH2:20][CH2:21][CH2:22][CH:15]2[C:16]2[C:17]([CH2:18]3)=[N:3][N:2]([CH3:1])[C:24]=2[OH:26])(=[O:13])=[O:12])=[CH:7][CH:6]=1Participants
5
Procedure
Prepared as described in Example using methylhydrazine and methyl 9-(4-chlorophenylsulfonyl)-3-oxo-9-azabicyclo[3.3.1]nonane-2-carboxylate, which was prepared as described in Example 12 using dimethyl carbonate and 9-(4-chlorophenylsulfonyl)-9-azabicyclo[3.3.1]nonan-3-one. See also: Bonjoch, Josep; Linares, Ana; Guardia, Manel; Bosch, Joan. Heterocycles 1987, 26(8), 2165-74.
Workup
- customPrepared
- customwas prepared
Sources & evidence
- ORD record
- ord-ff617f7553004a0595707df01809a863
- Source dataset
- uspto-grants-2008_03
- Patent number
- US07345056B2
Reaction notes
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