Diisopropylamine → HCID 21407935, compound
Reaction equation
[Cl:1][C:2]1[CH:30]=[CH:29][C:5]([O:6][CH:7]([O:11][C:12]2[CH:17]=[CH:16][C:15]([CH:18]3[C:27]4[C:22](=[CH:23][CH:24]=[CH:25][CH:26]=4)[N:21](C)[CH2:20][CH2:19]3)=[CH:14][CH:13]=2)[C:8]([OH:10])=[O:9])=[CH:4][CH:3]=1.C(NC(C)C)(C)C>>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([O:6][CH:7]([O:11][C:12]2[CH:17]=[CH:16][C:15]([CH:18]3[C:27]4[C:22](=[CH:23][CH:24]=[CH:25][CH:26]=4)[NH:21][CH2:20][CH2:19]3)=[CH:14][CH:13]=2)[C:8]([OH:10])=[O:9])=[CH:29][CH:30]=1Participants
3
Procedure
(4-chlorophenoxy)-[4-(1-methyl-1,2,3,4-tetrahydro-4-quinolyl)-phenoxy]-acetic acid,, diisopropylamine salt, m.p. 152°-155°;
Sources & evidence
- ORD record
- ord-0b6c328890e947e9b058dd63c55eb71d
- Source dataset
- uspto-grants-1977_09
- Patent number
- US04051170
Reaction notes
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