Tert-Butylamine → HCID 15549760, compound

HRID 2268816Notes

Reaction equation

HRID 2268816 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

  1. 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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