Hydrochloric Acid → 2-Amino-N-(2-chloro-1H-pyrrol-1-yl)acetamide Hydrochloride
Reaction equation
CC([N:5]([CH2:9][C:10]([NH:12][N:13]1[CH:17]=[CH:16][CH:15]=[C:14]1[Cl:18])=[O:11])C(=O)[O-])(C)C.Cl>CCOC(C)=O.CCOCC>[ClH:18].[NH2:5][CH2:9][C:10]([NH:12][N:13]1[CH:17]=[CH:16][CH:15]=[C:14]1[Cl:18])=[O:11]Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
To a stirred solution of 1,1-dimethylethyl-[2-(2-chloro-1H-pyrrol-1-ylamino)-2-oxoethyl]carbamate (3.1 g) in EtOAc (20 ml) and ether (20 ml) was added ethereal HCl (excess) at room temperature. The reaction mixture was allowed to stir for 19 hours at which time the precipitated product was filtered and washed with EtOAc. Recrystallization from ethanol/ether afforded 0.75 g of the product as a solid, m.p. 220° C. (dec.).
Workup
- filtrationwas filtered
- washwashed with EtOAc
- customRecrystallization from ethanol/ether
Sources & evidence
- ORD record
- ord-23ad1b9c0c0b4c8598d63af9462a37a2
- Source dataset
- uspto-grants-1995_06
- Patent number
- US05428053
Reaction notes
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