Ammonia → HCID 20184624, compound
Reaction equation
[CH2:1]([N:4]=[C:5]([NH2:19])[NH:6][C:7]1[CH:12]=[CH:11][N:10]=[C:9]([CH2:13][CH2:14][CH2:15][CH2:16][C:17]#[N:18])[N:8]=1)[CH2:2][CH3:3].S(=O)(=O)(O)[OH:21].N>>[CH2:1]([N:4]=[C:5]([NH2:19])[NH:6][C:7]1[CH:12]=[CH:11][N:10]=[C:9]([CH2:13][CH2:14][CH2:15][CH2:16][C:17]([NH2:18])=[O:21])[N:8]=1)[CH2:2][CH3:3]Participants
4
Procedure
A mixture of 5-(4-[2-propylguanidino]pyrimid-2-yl)valeronitrile (0.25 g.) and concentrated sulphuric acid (2 ml.) was stirred at ambient temperature for 3.5 hours. The reaction mixture was cooled in an ice bath and basified by careful dropwise addition of concentrated aqueous ammonia (s.g. 0.880). The resulting white precipitate was collected, washed with water and allowed to dry. The solid was purified by medium pressure chromatography on silica gel using CHCl3 /MeOH/aqueous ammonia (s.g. 0.880) 8:2:0.3 v/v/v as eluant to give 5-(4-[2-propylguanidino]pyrimid-2-yl)valeramide (0.15 g.), m.p. 212°-214°.
Workup
- customThe resulting white precipitate was collected
- washwashed with water
- customto dry
- customThe solid was purified by medium pressure chromatography on silica gel
Sources & evidence
- ORD record
- ord-8c9dd015cab2449f9bbf7d710673fdba
- Source dataset
- uspto-grants-1987_09
- Patent number
- US04696933
Reaction notes
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