HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2207318Generated: October 29, 2026
(2-(Methylthio)ethyl)amine → HCID 86654751, compound
https://huagongshe.com/reaction/2207318
Participants
| Role | Name | HCID | Charge |
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| Reactant | (2-(Methylthio)ethyl)amine | HCID 87697 | — |
| Reactant | HCID 86654752 | HCID 86654752 | — |
| Product | HCID 86654751 | HCID 86654751 | — |
Reaction Steps
Using a procedure similar to that described in Example 1, except using 5-[5-(3,5-bistrifluoromethylphenyl)-5-trifluoromethyl-4,5-dihydroisoxazol-3-yl]-imidazo[1,2-a]pyridine-8-carboxylic acid (45 mg) and 2-methylthioethylamine (0.016 mL), the title compound was isolated as an orange-reddish solid (11.9 mg, 23%). MS (ES): M/Z [M+H]=585. 1H NMR (400 MHz, CHLOROFORM-d): 2.22 (s, 3H), 2.85 (t, J=6.8 Hz, 2H), 3.82 (q, J=6.6 Hz, 2H), 4.01 (d, J=17.0 Hz, 1H), 4.44 (d, J=16.8 Hz, 1H), 7.21 (d, J=7.6 Hz, 1H), 7.85 (s, 1H), 8.02 (s, 1H), 8.12 (s, 2H), 8.28 (d, J=7.6 Hz, 1H), 8.90 (d, J=1.0 Hz, 1H), 10.67 (br. s., 1H). 19F NMR (376 MHz, CHLOROFORM-d): −80.0 (s, 3F), −63.3 (s, 6F). Compound No 2.004 of Example 7 was prepared according to the following general reaction Scheme 6:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09376434B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-1d369d05953140d1b65f41db237c79ee |
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| Source note | uspto-grants-2016_06 |
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