HuagongsheHuagongshe Chemistry Print Report · For research reference only
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
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-methyl-N-(3-methyl-benzo[b]thiophen-2-ylmethyl)acrylamide | HCID 17930139 | — |
| Reactant | N-(1-methyl-1H-indol-3-ylmethyl)-N-methylacrylamide | HCID 22139011 | — |
| Reactant | 7-Bromo-3,3-dimethyl-1,3,4,5-tetrahydropyrido[2,3-e][1,4]diazepin-2-one | HCID 59456914 | — |
| Reactant | 5-Bromo-3-morpholin-4-ylmethyl-pyridin-2-ylamine | HCID 66966248 | — |
| Product | (E)-3-(6-Amino-5-morpholin-4-ylmethyl-pyridin-3-yl)-N-methyl-N-(1-methyl-1H-indol-3-ylmethyl)acrylamide | HCID 66967319 | 38% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07879872B2 |
| Source dataset | uspto-grants-2011_02 |
| ORD ID | ord-cd6e842b2d4749aebeb754545ee0d043 |
| Source note | uspto-grants-2011_02 |