HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1362212Generated: October 29, 2026
methyl((1-methyl-1H-indol-2-yl)methyl)amine → HCID 10433701, compound
https://huagongshe.com/reaction/1362212
Participants
| Role | Name | HCID | Charge |
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| Reactant | methyl((1-methyl-1H-indol-2-yl)methyl)amine | HCID 11401058 | — |
| Reactant | Methyl-(1-propyl-naphthalen-2-ylmethyl)amine | HCID 59456959 | — |
| Reactant | (E)-3-(4-methyl-2-oxo-2,3,4,5-tetrahydro-1H-pyrido[2,3-e][1,4]diazepin-7-yl)acrylic acid hydrochloride | HCID 66966197 | — |
| Reactant | HCID 66966913 | HCID 66966913 | — |
| Product | HCID 10433701 | HCID 10433701 | 22% |
Reaction Steps
According to the procedure of Example 1 (a), except substituting (E)-3-[3-(2-dimethylamino-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, and substituting methyl-(1-methyl-1H-indol-2-ylmethyl)amine for the methyl-(1-propyl-naphthalen-2-ylmethyl)amine, the title compound (40 mg, 22%) was prepared as a pale yellow solid: 1H NMR (300 MHz, DMSO-d6) δ 9.98 (br s, 1H), 8.38-8.33 (m, 1H), 8.00-7.91 (m, 1H), 7.57-7.42 (m, 3H), 7.22-7.01 (m, 3H), 6.42-6.16 (m, 1H), 5.04-4.85 (m, 2H), 4.53-4.47 (m, 2H), 3.72-3.68 (m, 3H), 3.51-3.31 (m, 4H), 3.11-2.99 (m, 4H), 2.72-2.39 (m, 5H); MS (ESI) m/e 447 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07879872B2 |
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| Source dataset | uspto-grants-2011_02 |
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| ORD ID | ord-4b66fa91dda7429da30d01c500594553 |
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| Source note | uspto-grants-2011_02 |
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