Ammonia → HCID 20184624, compound

HRID 2309710Notes

Reaction equation

HRID 2309710 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

  1. customThe resulting white precipitate was collected
  2. washwashed with water
  3. customto dry
  4. 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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