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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1920772Generated: October 29, 2026

N-Ethyl-N-methylcarbamoyl chloride → HCID 44455199, compound

https://huagongshe.com/reaction/1920772

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-Ethyl-N-methylcarbamoyl chlorideHCID 11240471—
ReactantHCID 67493078HCID 67493078—
ProductHCID 44455199HCID 4445519950%

Reaction Steps

7-Hydroxy-N-cyclopropylmethyl-1,2,3,4-tetrahydroisoquinoline (9) was mixed homogeneously with N-ethyl-N-methyl-carbamoyl chloride (10a) and carried out step (f-2). Purified on a silica gel column (DCM/MeOH=10:1) gave cyclopropylmethyl- and N-Ethyl-N-methyl amino-containing 7-(N-Methyl-N-ethyl-carbamoyloxy)-N-cyclopropylmethyl-1,2,3,4-tetrahydroisoquinoline (12a) (Yield 50%). 1H NMR (300 MHz, CDCl3) (NMR, Varian Gemini): δ 7.06 (d, J=8 Hz, 1H, Aryl H); 6.84 (s, 1H, Aryl H); 6.81 (s, 1H, Aryl H): 3.71 (s, 2H, Ph-CH2—N); δ 3.44, 3.39 (dd, J=7 Hz, 2H, CH3—N—CH2CH3); 3.03-2.75 (m, 7H, CH3—N—CH2—CH3, Ph-CH2—CH2—N); 2.42 (d, J=6 Hz, 2H, N—CH2); 1.24-1.17 (m, 3H, —CH3); 1.14-0.94 (q, J=7 Hz, 1H); 0.58-0.52 (m, 2H); 0.19-0.14 (m, 2H); IR (KBr): ν cm−1=2924, 1715. Fast Atom Bombardment Mass Spectrometry (FABMS) m/z: 289 (M+1) (C17H24N2O2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08173648B2
Source datasetuspto-grants-2012_05
ORD IDord-2b6943175d0e4d99af2295418a44bfa2
Source noteuspto-grants-2012_05