2-(Diisopropylamino)ethyl chloride → HCID 19354035, compound

HRID 377252Notes

Reaction equation

HRID 377252 reaction equation
[F:1][C:2]([F:33])([F:32])[C:3]1[CH:31]=[CH:30][CH:29]=[CH:28][C:4]=1[CH2:5][N:6]1[C:10]2[CH:11]=[C:12]([OH:15])[CH:13]=[CH:14][C:9]=2[N:8]=[C:7]1[C:16]1[CH:21]=[C:20]([O:22][CH3:23])[C:19]([O:24][CH3:25])=[C:18]([O:26][CH3:27])[CH:17]=1.[CH:34]([N:37]([CH2:41][CH2:42]Cl)[CH:38]([CH3:40])[CH3:39])([CH3:36])[CH3:35]>>[F:33][C:2]([F:1])([F:32])[C:3]1[CH:31]=[CH:30][CH:29]=[CH:28][C:4]=1[CH2:5][N:6]1[C:10]2[CH:11]=[C:12]([O:15][CH2:42][CH2:41][N:37]([CH:38]([CH3:40])[CH3:39])[CH:34]([CH3:36])[CH3:35])[CH:13]=[CH:14][C:9]=2[N:8]=[C:7]1[C:16]1[CH:17]=[C:18]([O:26][CH3:27])[C:19]([O:24][CH3:25])=[C:20]([O:22][CH3:23])[CH:21]=1

Participants

3

Reactant 2

HCID 73122-(Diisopropylamino)ethyl chlorideHCID 15388688HCID 15388688, compound

Product 1

HCID 19354035HCID 19354035, compound

Procedure

The title compound was prepared by reacting the compound of Example 104 with 2-(N,N-diisopropylamino)ethyl chloride essentially as previously described. mp 184° C., MS 585, NMR, IR.

Sources & evidence

ORD record
ord-c4e2bd788a38438185c4d137523350d1
Source dataset
uspto-grants-2000_02
Patent number
US06025379

Reaction notes

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