Thionyl Chloride → HCID 178490036, compound
Reaction equation
[CH2:1]([C:10]1([OH:24])[C:18]2[C:13](=[CH:14][CH:15]=[CH:16][CH:17]=2)[N:12]=[C:11]1[NH:19][CH2:20][CH2:21][CH2:22]O)[C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([O:8][CH3:9])[CH:3]=1.S(Cl)([Cl:27])=O>>[CH2:1]([C:10]1([OH:24])[C:18]2[C:13](=[CH:14][CH:15]=[CH:16][CH:17]=2)[N:12]=[C:11]1[NH:19][CH2:20][CH2:21][CH2:22][Cl:27])[C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([O:8][CH3:9])[CH:3]=1Participants
3
Procedure
Reaction of 3-(m-anisyl)-2-(3-hydroxypropylamino)-3H-indol-3-ol with thionylchloride by a procedure analogous to that described in Example 2 gives 3-(m-anisyl)-2-(3-chloropropylamino)-3H-indol-3-ol.
Sources & evidence
- ORD record
- ord-563cb18a1f8a40cfa48c20568f09795e
- Source dataset
- uspto-grants-1976_05
- Patent number
- US03957819
Reaction notes
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