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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1362239Generated: October 29, 2026

N-methyl-N-(3-methyl-benzo[b]thiophen-2-ylmethyl)acrylamide → (E)-3-(6-Amino-5-morpholin-4-ylmethyl-pyridin-3-yl)-N-methyl-N-(1-methyl-1H-indol-3-ylmethyl)acrylamide

https://huagongshe.com/reaction/1362239

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-methyl-N-(3-methyl-benzo[b]thiophen-2-ylmethyl)acrylamideHCID 17930139—
ReactantN-(1-methyl-1H-indol-3-ylmethyl)-N-methylacrylamideHCID 22139011—
Reactant7-Bromo-3,3-dimethyl-1,3,4,5-tetrahydropyrido[2,3-e][1,4]diazepin-2-oneHCID 59456914—
Reactant5-Bromo-3-morpholin-4-ylmethyl-pyridin-2-ylamineHCID 66966248—
Product(E)-3-(6-Amino-5-morpholin-4-ylmethyl-pyridin-3-yl)-N-methyl-N-(1-methyl-1H-indol-3-ylmethyl)acrylamideHCID 6696731938%

Reaction Steps

According to the procedure of Example 2(a), except substituting N-methyl-N-(1-methyl-1H-indol-3-ylmethyl)acrylamide for the N-methyl-N-(3-methyl-benzo[b]thiophen-2-ylmethyl)acrylamide, and substituting 5-bromo-3-morpholin-4-ylmethyl-pyridin-2-ylamine for the 7-bromo-3,3-dimethyl-1,3,4,5-tetrahydro-pyrido[2,3-e][1,4]diazepin-2-one, the title compound (510 mg, 38%) was prepared as an off-white powder: 1H NMR (300 MHz, DMSO-d6) δ 8.13 (s, 1H),7.78 (s, 1H), 7.63-6.91 (m, 7H), 6.51 (s, 2H), 4.89-4.72 (m, 2H), 3.76 (s, 3H), 3.57 (br s, 4H), 3.42-3.34 (m, 2H), 3.02-2.90 (m, 3H), 2.33 (br s, 4H); MS (ESI) m/e 420 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07879872B2
Source datasetuspto-grants-2011_02
ORD IDord-cd6e842b2d4749aebeb754545ee0d043
Source noteuspto-grants-2011_02