Cyclopropanecarboximidamide hydrochloride → HCID 23440938, compound

HRID 2119948Notes

Reaction equation

HRID 2119948 reaction equation
CN([CH:4]=[C:5]1[C:11](=O)[C:10]2[CH:13]=[CH:14][CH:15]=[CH:16][C:9]=2[NH:8][C:7](=[O:17])[CH2:6]1)C.Cl.[CH:19]1([C:22]([NH2:24])=[NH:23])[CH2:21][CH2:20]1>>[CH:19]1([C:22]2[N:23]=[CH:4][C:5]3[CH2:6][C:7](=[O:17])[NH:8][C:9]4[CH:16]=[CH:15][CH:14]=[CH:13][C:10]=4[C:11]=3[N:24]=2)[CH2:21][CH2:20]1

Participants

3

Reactant 2

HCID 2781916Cyclopropanecarboximidamide hydrochlorideHCID 669347634-dimethylaminomethylene-3,4-dihydro-1H-benzo[b]azepine-2,5-dione

Product 1

HCID 23440938HCID 23440938, compoundYield 62%

Procedure

Analogous to Scheme 1 from 4-[(dimethylamino)methylene]-3,4-dihydro-1H-benzazepine-2,5-dione and cyclopropanecarboxamidine hydrochloride. Yield: 62%.

Sources & evidence

ORD record
ord-f08c2d6f64a148249a157ef2e6a937cf
Source dataset
uspto-grants-2004_02
Patent number
US06686352B2

Reaction notes

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