Tert-Butylamine → HCID 15549760, compound
Reaction equation
Cl[C:2]1[N:7]2[N:8]=[CH:9][C:10]([C:11]#[N:12])=[C:6]2[N:5]=[C:4]([C:13]([O:15][CH2:16][CH3:17])=[O:14])[C:3]=1[CH2:18][CH2:19]Cl.[C:21]([NH2:25])([CH3:24])([CH3:23])[CH3:22]>>[C:21]([N:25]1[C:2]2[N:7]3[N:8]=[CH:9][C:10]([C:11]#[N:12])=[C:6]3[N:5]=[C:4]([C:13]([O:15][CH2:16][CH3:17])=[O:14])[C:3]=2[CH2:18][CH2:19]1)([CH3:24])([CH3:23])[CH3:22]Participants
3
Procedure
The intended compound was obtained in the same manner as in Synthesis Example (5) using ethyl 7-chloro-6-(2-chloroethyl)-3-cyanopyrazolo[1,5-a]pyrimidine-5-carboxylate and tert-butylamine.
Workup
- customThe intended compound was obtained in the same manner as in Synthesis Example (5)
Sources & evidence
- ORD record
- ord-7245ad2ac752480f8e68b855fd5f8e20
- Source dataset
- uspto-grants-2001_12
- Patent number
- US06329382B1
Reaction notes
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