HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2201075Generated: October 27, 2026
Potassium Carbonate → HCID 67773713, compound
https://huagongshe.com/reaction/2201075
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Binap, (A+-)- | HCID 634876 | — |
| Reactant | 3-Methylisothiazol-5-ylamine hydrochloride | HCID 2723918 | — |
| Reactant | (R)-tert-butyl 1-(3-bromo-4-cyanophenylamino)-3-methoxypropan-2-ylcarbamate | HCID 67775752 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Product | HCID 67773713 | HCID 67773713 | — |
Reaction Steps
A mixture of (R)-tert-butyl 1-(3-bromo-4-cyanophenylamino)-3-methoxypropan-2-ylcarbamate (150 mg, 0.39 mmol), 5-amino-3-methylisothiazole hydrochloride (76 mg, 0.51 mmol), BINAP (25 mg, 0.04 mmol), Pd(OAc)2 (18 mg, 0.08 mmol) and K2CO3 (188 mg, 1.37 mmol) p-dioxane (3 mL) was degassed with Ar, then was heated at 120° C. for 15 h. the mixture was filtered, filter cake was washed with EtOAc, and the filtrated was concentrated in vacuo to give (R)-tert-butyl 1-(4-cyano-3-(3-methylisothiazol-5-ylamino)phenylamino)-3-methoxypropan-2-ylcarbamate as crude oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09359375B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-4be91f9bec3d45d7b4c22863d017833c |
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| Source note | uspto-grants-2016_06 |
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