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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1362233Generated: October 25, 2026

(3-Methoxy-2-propoxybenzyl)methylamine → HCID 66967398, compound

https://huagongshe.com/reaction/1362233

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(3-Methoxy-2-propoxybenzyl)methylamineHCID 28338626—
ReactantMethyl-(1-propyl-naphthalen-2-ylmethyl)amineHCID 59456959—
Reactant(E)-3-[3-(2-morpholin-4-yl-ethyl)-2-oxo-1,2,3,4-tetrahydro-pyrido[2,3-d]pyrimidin-6-yl]acrylic acid hydrochlorideHCID 66967508—
ProductHCID 66967398HCID 6696739835%

Reaction Steps

According to the procedure of Example 1, except substituting 3-methoxy-2-propoxy-benzyl-methylamine for the methyl-(1-propyl-naphthalen-2-ylmethyl)amine, and substituting (E)-3-[3-(2-morpholin-4-yl-ethyl)-2-oxo-1,2,3,4-tetrahydro-pyrido[2,3-d]pyrimidin-6-yl]acrylic acid hydrochloride for the (E)-3-(4-methyl-2-oxo-2,3,4,5-tetrahydro-1H-pyrido[2,3,-e][1,4]diazepin-7-yl)acrylic acid hydrochloride, the title compound (0.10 g, 35%) was prepared as an off-white solid: 1H NMR (300 MHz, DMSO-d6) δ 10.68 (br s, 1H), 10.13 (m, 1H), 8.40-8.30 (m, 1H), 8.01-7.90 (m, 1H), 7.60-7.42 (m, 1H), 7.29-7.15 (m, 1H), 7.01-6.90 (m, 2H), 6.70-6.60 (m, 1H), 4.80-4.51 (m, 4H), 4.02-3.70 (m, 10H), 3.60-3.50 (m, 2H), 3.42-3.30 (m, 2H), 3.20-2.87 (m, 6H), 1.74-1.67 (m, 2H), 1.00-0.91 (m, 3H); MS (ESI) m/e 524 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07879872B2
Source datasetuspto-grants-2011_02
ORD IDord-4d5e8e5141544676aa318a8037ea4bea
Source noteuspto-grants-2011_02