Hydrochloric Acid → HCID 54209856, compound
Reaction equation
[O:1]1[CH:6]=[CH:5][CH2:4][CH2:3][CH2:2]1.[OH:7][C:8]1[CH:21]=[CH:20][C:19]2[S:18][C:17]3[C:12](=[CH:13][CH:14]=[CH:15][C:16]=3[S:22](=[O:27])(=[O:26])[N:23]([CH3:25])[CH3:24])[N:11]([CH2:28][CH2:29][CH2:30][Cl:31])[C:10]=2[CH:9]=1.Cl>C(O)C>[O:1]1[CH2:2][CH2:3][CH2:4][CH2:5][CH:6]1[O:7][C:8]1[CH:21]=[CH:20][C:19]2[S:18][C:17]3[C:12](=[CH:13][CH:14]=[CH:15][C:16]=3[S:22](=[O:26])(=[O:27])[N:23]([CH3:24])[CH3:25])[N:11]([CH2:28][CH2:29][CH2:30][Cl:31])[C:10]=2[CH:9]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
15.7 g.) is prepared by reacting dihydropyran (102 g.) with 2-hydroxy-6-dimethylsulphamoyl-10-(3-chloropropyl)-phenothiazine (17.2 g.) in the presence of an 8N solution of hydrogen chloride in ethanol (0.1 cc.).
Workup
- custom) is prepared
Sources & evidence
- ORD record
- ord-22687ae0728f4691998c0fbb2a1cb0d5
- Source dataset
- uspto-grants-1976_06
- Patent number
- US03961055
Reaction notes
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