Pentylamine → HCID 12043759, compound
Reaction equation
Cl[C:2]1[C:3]2[CH2:12][O:11][CH2:10][CH2:9][C:4]=2[N:5]=[C:6]([NH2:8])[N:7]=1.[CH2:13]([NH2:18])[CH2:14][CH2:15][CH2:16][CH3:17]>>[NH2:8][C:6]1[N:7]=[C:2]([NH:18][CH2:13][CH2:14][CH2:15][CH2:16][CH3:17])[C:3]2[CH2:12][O:11][CH2:10][CH2:9][C:4]=2[N:5]=1Participants
3
Procedure
A mixture of 4-chloro-7,8-dihydro-5H-pyrano[4,3-d]pyrimidine-2-ylamine (29.3 mg, 0.158 mmol) and amylamine (1.0 ml) was refluxed for 2.5 hours. After reaction, the procedure according to pro-treatment of Example 7 was carried out to give the object compound (22.3 mg, 59%).
Workup
- temperaturewas refluxed for 2.5 hours
- customAfter reaction
Sources & evidence
- ORD record
- ord-ea9967d56962415795864ef0bea23854
- Source dataset
- uspto-grants-2002_10
- Patent number
- US06458798B1
Reaction notes
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