HCID 10769106, compound → HCID 22106653, compound

HRID 1456862Notes

Reaction equation

HRID 1456862 reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([C:20]([C:26]2[CH:31]=[CH:30][C:29]([O:32][CH2:33][C:34]3[CH:43]=[CH:42][C:41]4[C:36](=[CH:37][CH:38]=[CH:39][CH:40]=4)[N:35]=3)=[C:28]([Cl:44])[CH:27]=2)([CH3:25])[CH2:21][CH2:22][CH2:23][OH:24])[CH:5]=[CH:6][C:7]=1[O:8][CH2:9][C:10]1[CH:19]=[CH:18][C:17]2[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=2)[N:11]=1.[N:45]1C2C(=CC=CC=2)C=CC=1COC1C=CC(C(C2C=CC(OCC3C=CC4C(=CC=CC=4)N=3)=CC=2)(C)CCCO)=CC=1>>[Cl:44][C:28]1[CH:27]=[C:26]([C:20]([C:4]2[CH:5]=[CH:6][C:7]([O:8][CH2:9][C:10]3[CH:19]=[CH:18][C:17]4[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=4)[N:11]=3)=[C:2]([Cl:1])[CH:3]=2)([CH3:25])[CH2:21][CH2:22][CH2:23][O:24][NH2:45])[CH:31]=[CH:30][C:29]=1[O:32][CH2:33][C:34]1[CH:43]=[CH:42][C:41]2[C:36](=[CH:37][CH:38]=[CH:39][CH:40]=2)[N:35]=1

Participants

3

Reactant 2

HCID 10769106HCID 10769106, compoundHCID 22106657HCID 22106657, compound

Product 1

HCID 22106653HCID 22106653, compound

Procedure

The desired compound was prepared according to the method of Example 5, steps 1 and 2, except substituting 4,4-bis(3-chloro-4-(2-quinolylmethoxy)phenyl)pentan-1-ol, prepared as in step 1, for 4,4-bis(4-(2-quinolylmethoxy)phenyl)pentan-1-ol.

Sources & evidence

ORD record
ord-18838f192880441298d988ba7580a29b
Source dataset
uspto-grants-1998_12
Patent number
US05843968

Reaction notes

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