HuagongsheHuagongshe Chemistry Print Report · For research reference only
methyl((1-methyl-1H-indol-2-yl)methyl)amine → HCID 66966327, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| 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 66967448 | HCID 66967448 | — |
| Product | HCID 66966327 | HCID 66966327 | 23% |
Reaction Steps
According to the procedure of Example 1, except substituting 3-[6-amino-5-(2-morpholin-4-yl-ethylcarbamoyl)pyridin-3-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 methyl-(1-methyl-1H-indol-2-ylmethyl)amine for the methyl-(1-propyl-naphthalen-2-ylmethyl)amine, the title compound (170 mg, 23%) was prepared as a pale yellow solid: 1H NMR (300 MHz, DMSO-d6) δ 10.87-10.61 (m, 1H), 9.69-9.66 (m, 1H), 9.40-9.28 (m, 1H), 8.70-8.31 (m, 3H), 7.95-7.39 (m, 4H), 7.15-6.97 (m, 2H), 6.40-6.08 (m, 1H), 5.27-4.85 (m, 2H), 3.94-3.55 (m, 12H), 3.20-2.96 (m, 6H); MS (ESI) m/e 477 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07879872B2 |
| Source dataset | uspto-grants-2011_02 |
| ORD ID | ord-84064e261781422c8ac87d12b8edc281 |
| Source note | uspto-grants-2011_02 |