HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 59524Generated: October 29, 2026
Pivaloyl chloride → HCID 136492440, compound
https://huagongshe.com/reaction/59524
Participants
| Role | Name | HCID | Charge |
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| Reactant | Pivaloyl chloride | HCID 62493 | — |
| Reactant | HCID 136492384 | HCID 136492384 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Diisopropylethylamine | HCID 81531 | — |
| Product | HCID 136492440 | HCID 136492440 | 47.3% |
Reaction Steps
To a solution of 5-(5-(aminomethyl)-2-chlorophenyl)-2-(4,4-dimethylcyclohexyl)-2H-1,2,4-triazol-3(4H)-one (Intermediate-73, 0.070 g, 0.202 mmol) in dry THF (5.0 mL), DIPEA (2.0 mL) and pivaloyl chloride (0.30 g, 0.242 mmol) were added and the reaction mass was stirred at RT for 16 h. After completion of the reaction, the reaction mass was quenched with water and extracted with 10%.MeOH:DCM. The organic layer was washed with dilute HCl and concentrated. The obtained crude was purified with column chromatography on basic alumina by eluting with 2.0% MeOH:DCM to afford 0.040 g of the desired product. 1H NMR (300 MHz, DMSO d6): δ 1.44 (s, 6H), 1.47 (s, 9H), 1.81-1.94 (m, 8H), 3.86-3.90 (m, 1H), 4.40 (s, 2H), 7.33 (d, J=1.5 Hz, 1H), 7.45 (s, 7.50 (d, J=2.1 Hz, 1H), 8.16 (t, 1H), 11.93 (s, 1H); MS (m/z): 419.21 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09439890B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-022f92c8bb104a42ac883ae8cc195991 |
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| Source note | uspto-grants-2016_09 |
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