HuagongsheHuagongshe Chemistry Print Report · For research reference only
(2-(Methylthio)ethyl)amine → HCID 53252790, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (2-(Methylthio)ethyl)amine | HCID 87697 | — |
| Reactant | HCID 67247370 | HCID 67247370 | — |
| Product | HCID 53252790 | HCID 53252790 | — |
Reaction Steps
Using a procedure similar to that described in Example 1, except using 5-[5-(3,5-dichlorophenyl)-5-trifluoromethyl-4,5-dihydroisoxazol-3-yl]-indolizine-8-carboxylic acid (37 mg, described above in Example 3) and 2-methylthioethylamine, the title compound was isolated as an orange-reddish solid (21.2 mg, 49%). MS (ES): M/Z [M+H]=516. 1H NMR (400 MHz, CHLOROFORM-d): 2.17 (s, 3H), 2.83 (t, J=6.2 Hz, 2H), 3.75 (q, J=6.0 Hz, 2H), 3.91 (d, J=16.6 Hz, 1H), 4.28 (d, J=16.6 Hz, 1H), 6.83 (d, J=7.4 Hz, 1H), 7.02-7.08 (m, 1H), 7.17 (d, J=7.2 Hz, 1H), 7.46 (t, J=1.7 Hz, 1H), 7.55 (s, 2H), 8.73 (d, J=1.6 Hz, 1H). 19F NMR (376 MHz, CHLOROFORM-d): −79.8 (s, 3F).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09376434B2 |
| Source dataset | uspto-grants-2016_06 |
| ORD ID | ord-43f35a4e996c45068002cee866fe2ed5 |
| Source note | uspto-grants-2016_06 |