Cyclopropylamine → HCID 18630189, compound
Reaction equation
[CH2:1]([NH:3][C:4](=[O:16])[C:5]1[C:10]([Si:11]([CH3:14])([CH3:13])[CH3:12])=[CH:9][CH:8]=[CH:7][C:6]=1[I:15])[CH3:2].[CH:17]1(N)CC1>>[CH:1]1([NH:3][C:4](=[O:16])[C:5]2[C:10]([Si:11]([CH3:14])([CH3:13])[CH3:12])=[CH:9][CH:8]=[CH:7][C:6]=2[I:15])[CH2:17][CH2:2]1Participants
3
Procedure
The acid chloride prepared in Example 207 was reacted with cyclopropylamine (3 eq) using General Method El to afford the title compound. Purification by recrystallization from hexanes gave 0.49 g of the title compound as white needles in 87% yield. m.p. 162-164° C.
Sources & evidence
- ORD record
- ord-81e6d205ba2e48f4a64debbbe43917c1
- Source dataset
- uspto-grants-2000_02
- Patent number
- US06028101
Reaction notes
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