Formaldehyde → HCID 18962079, compound
Reaction equation
[CH:1]1([NH:7][CH:8]2[CH2:13][CH2:12][CH2:11][CH2:10][CH2:9]2)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[CH2:14]=O.[Cl:16][C:17]1[CH:18]=[C:19]([C:29]#[CH:30])[CH:20]=[CH:21][C:22]=1[CH:23]1[CH2:28][CH2:27][CH2:26][CH2:25][CH2:24]1>>[ClH:16].[CH:8]1([N:7]([CH2:14][C:30]#[C:29][C:19]2[CH:20]=[CH:21][C:22]([CH:23]3[CH2:28][CH2:27][CH2:26][CH2:25][CH2:24]3)=[C:17]([Cl:16])[CH:18]=2)[CH:1]2[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6]2)[CH2:9][CH2:10][CH2:11][CH2:12][CH2:13]1Participants
4
Procedure
This compound is prepared, following the procedure described in Example I, by reacting dicyclohexylamine and paraformaldehyde with 3-chloro-4-cyclohexyl-1 -ethynylbenzene.
Workup
- customThis compound is prepared
Sources & evidence
- ORD record
- ord-52623d9ce5e44b68889cb4c8a44c731f
- Source dataset
- uspto-grants-1994_10
- Patent number
- US05354781
Reaction notes
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