Methanesulfonyl chloride → HCID 20039837, compound
Reaction equation
[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]2[CH2:13][CH2:12][N:11]([C:14]3[N:15]([CH3:20])[C:16]([CH3:19])=[CH:17][N:18]=3)[CH2:10][CH2:9]2)=[CH:4][CH:3]=1.[CH3:21][S:22](Cl)(=[O:24])=[O:23]>N1C=CC=CC=1>[CH3:20][N:15]1[C:16]([CH3:19])=[CH:17][N:18]=[C:14]1[N:11]1[CH2:10][CH2:9][CH:8]([C:5]2[CH:6]=[CH:7][C:2]([NH:1][S:22]([CH3:21])(=[O:24])=[O:23])=[CH:3][CH:4]=2)[CH2:13][CH2:12]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Treatment of the product from part (ii) above (0.46 g) with methanesulphonyl chloride (0.22 g) in pyridine (12 ml) according to the method fo Example 1(iii) gave the title compound, (0.40 g), m.p. 225°-226°.
Sources & evidence
- ORD record
- ord-1a0100c044804068aa3b408cba9e1fc3
- Source dataset
- uspto-grants-1989_05
- Patent number
- US04835165
Reaction notes
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