Ammonia → HCID 19709716, compound
Reaction equation
C([O:4][CH:5]([CH3:18])[CH2:6][CH2:7][C:8]1[CH:13]=[C:12](Cl)[N:11]2[N:15]=[CH:16][CH:17]=[C:10]2[N:9]=1)(=O)C.[NH3:19]>>[NH2:19][C:12]1[N:11]2[N:15]=[CH:16][CH:17]=[C:10]2[N:9]=[C:8]([CH2:7][CH2:6][CH:5]([OH:4])[CH3:18])[CH:13]=1Participants
3
Conditions
- Temperature
- 105 °C
Procedure
The compound prepared in step (5) (4.3 g) and 25% aqueous ammonia (50 ml) were enclosed in a stainless steel sealed tube, heated at 105° C. for 14 hours and allowed to cool. The crystals precipitated were collected by filtration, washed with water and dried to provide 3.2 g of 7-amino-5-(3-hydroxybutyl)pyrazolo[1,5-a]pyrimidine as light yellow crystals.
Workup
- temperatureto cool
- customThe crystals precipitated
- filtrationwere collected by filtration
- washwashed with water
- customdried
Sources & evidence
- ORD record
- ord-32e7768f154d492e9fbf990d7550b48a
- Source dataset
- uspto-grants-1998_01
- Patent number
- US05707997
Reaction notes
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