2-(Diisopropylamino)ethyl chloride → HCID 19353982, compound

HRID 377257Notes

Reaction equation

HRID 377257 reaction equation
[Br:1][C:2]1[CH:30]=[CH:29][CH:28]=[CH:27][C:3]=1[CH2:4][N:5]1[C:9]2[CH:10]=[C:11]([OH:14])[CH:12]=[CH:13][C:8]=2[N:7]=[C:6]1[C:15]1[CH:20]=[C:19]([O:21][CH3:22])[C:18]([O:23][CH3:24])=[C:17]([O:25][CH3:26])[CH:16]=1.[CH:31]([N:34]([CH2:38][CH2:39]Cl)[CH:35]([CH3:37])[CH3:36])([CH3:33])[CH3:32]>>[Br:1][C:2]1[CH:30]=[CH:29][CH:28]=[CH:27][C:3]=1[CH2:4][N:5]1[C:9]2[CH:10]=[C:11]([O:14][CH2:39][CH2:38][N:34]([CH:35]([CH3:37])[CH3:36])[CH:31]([CH3:33])[CH3:32])[CH:12]=[CH:13][C:8]=2[N:7]=[C:6]1[C:15]1[CH:16]=[C:17]([O:25][CH3:26])[C:18]([O:23][CH3:24])=[C:19]([O:21][CH3:22])[CH:20]=1

Participants

3

Reactant 2

HCID 73122-(Diisopropylamino)ethyl chlorideHCID 19354036HCID 19354036, compound

Product 1

HCID 19353982HCID 19353982, compound

Procedure

The title compound was prepared by reacting the compound of Example 114 with 2-(N,N-diisopropylamino)ethyl chloride essentially as previously described MS 595, 597.

Sources & evidence

ORD record
ord-c17624392fe347b3ad6d0be0a5984f9b
Source dataset
uspto-grants-2000_02
Patent number
US06025379

Reaction notes

Loading…