Acetamidine monohydrochloride → HCID 178433460, compound
Reaction equation
[Na].Cl.[C:3]([NH2:6])(=[NH:5])[CH3:4].C[CH2:8][CH:9]([C:14](OCC)=[O:15])[C:10](OC)=[O:11]>CO>[CH3:4][C:3]1[N:6]=[C:10]([OH:11])[C:9]([CH3:8])=[C:14]([OH:15])[N:5]=1Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 23 °C
Procedure
According to the procedure of D. J. Brown et al., J. Chem. Soc. 1964, 3204, a solution of 9.2 g (400 mmol) of sodium metal dissolved in 200 mL of methanol was treated first with 19.8 g. (210 mmol) of acetamidine hydrochloride and then with 34.4 mL (34.8 g, 200 mmol) of diethyl methyl malonate. The reaction mixture was heated to reflux for 4 hours, cooled to 23° C., and filtered. The filtrate was concentrated in vacuo. The residue from the filtrate and the isolated solids were combined and dissolved in water (300 mL). The aqueous solution was acidified with aqueous 3N HCl (133 mL). The fine white solid which precipitated from this solution was isolated by filtration and dried in vacuo to give 24.9 g (89%) of pure product, m.p. 300° C.
Workup
- additionwas treated first with 19.8 g
- temperatureThe reaction mixture was heated
- temperatureto reflux for 4 hours
- filtrationfiltered
- concentrationThe filtrate was concentrated in vacuo
- dissolutiondissolved in water (300 mL)
- customThe fine white solid which precipitated from this solution
- customwas isolated by filtration
- customdried in vacuo
Sources & evidence
- ORD record
- ord-3f8b4e9cdc9b47e5bcc595e897d380a4
- Source dataset
- uspto-grants-1986_10
- Patent number
- US04617393
Reaction notes
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