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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 729640Generated: October 29, 2026

HCID 1476965, compound → HCID 57833087, compound

https://huagongshe.com/reaction/729640

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 1476965HCID 1476965—
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 86622701HCID 86622701—
SolventMethanolHCID 887—
ProductHCID 57833087HCID 5783308758.3%

Reaction Steps

3-[(Dimethylamino)methylene]-1-methylpiperidin-4-one (9.04 g, 53.7 mmol) and tert-butyl {(3R)-1-[amino(imino)methyl]pyrrolidin-3-yl}carbamate hydrochloride (14.2 g, 53.7 mmol) were dissolved in methanol (100 mL) and to this was added dropwise sodium methoxide (9.66 g of a 30% solution in methanol). The reaction mixture was refluxed for 3 hours and then cooled to room temperature. The reaction mixture was then evaporated to dryness, and the residue was treated with water (50 mL). The precipitate was separated by filtration, washed with water (25 mL) and diethyl ether (50 mL) and dried to give the title compound 10.43 g (yield 58%). LCMS (ES+) M+H 334. 1H NMR (DMSO-d6) 1.39 (s, 9H) 1.85 (m, 1H) 2.13 (m, 1H) 2.33 (s, 3H) 2.60 (m, 2H) 2.67 (m, 2H) 3.23-3.26 (m, 1H) 3.31-3.37 (m, 3H) 3.40-3.536 (m, 1H) 3.63 (m, 1H) 4.04 (br s, 1H) 7.20 (br s, 1H) 8.04 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07582643B2
Source datasetuspto-grants-2009_09
ORD IDord-a379dd958560455bb00541f01fa20352
Source noteuspto-grants-2009_09