Sulfamide → HCID 21247719, compound
Reaction equation
[CH2:1]([CH:6]1[CH2:11][O:10][CH:9]([C:12]2[CH:20]=[CH:19][C:15]([C:16](Cl)=O)=[CH:14][CH:13]=2)[CH2:8][CH2:7]1)[CH2:2][CH2:3][CH2:4][CH3:5].S(N)([NH2:24])(=O)=O>C1S(=O)(=O)CCC1>[C:16]([C:15]1[CH:19]=[CH:20][C:12]([CH:9]2[CH2:8][CH2:7][CH:6]([CH2:1][CH2:2][CH2:3][CH2:4][CH3:5])[CH2:11][O:10]2)=[CH:13][CH:14]=1)#[N:24]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of 29.5 g of p-(5-pentyl-2-tetrahydropyranyl)benzoyl chloride and 8 g of sulfamide in 500 ml of tetramethylene sulfone is heated at 120° for 4 hours, evaporated and worked up as usual. 2-p-cyanophenyl-5-pentyltetrahydropyran is obtained.
Workup
- customevaporated
Sources & evidence
- ORD record
- ord-5586723f6cf64843957c7580ea84c56b
- Source dataset
- uspto-grants-1989_04
- Patent number
- US04818431
Reaction notes
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