HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 473975Generated: October 30, 2026
Acetonitrile → 2-(cis-2,6-Dimethyl-morpholin-4-yl)-thiazole-4-carbonitrile
https://huagongshe.com/reaction/473975
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 4-(4-Bromo-thiazol-2-yl)-cis-2,6-dimethyl-morpholine | HCID 67216896 | — |
| Catalyst | Zinc cyanide (Zn(CN)2) | HCID 11186 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Product | 2-(cis-2,6-Dimethyl-morpholin-4-yl)-thiazole-4-carbonitrile | HCID 67216017 | 60% |
Reaction Steps
A mixture of Intermediate 1 (52.8 g, 190.49 mmol), triphenylphosphine (4.99 g, 19.05 mmol), zinc cyanide (22.37 g, 190.49 mmol) and dry acetonitrile (360 mL) was introduced in a pressure tube and was degassed with nitrogen for 5 min. Tetrakis(triphenylphosphine)palladium (11 g, 9.52 mmol) was added and the mixture was further degassed for 5 min. The tube was sealed and the reaction mixture was stirred at 140° C. for 3 h. The suspension was evaporated and taken up in water/DCM. The combined organic layer was separated, filtered on a plug of diatomaceous earth, dried on MgSO4, filtered off, and evaporated. The residue was purified on an 800 g EasyVarioPrep (Merck) column (eluent: DCM). The desired fractions were concentrated in vacuo and dried in a vacuum oven at 50° C. overnight, yielding 25.6 g (60%) of Intermediate 2 as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08637510B2 |
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| Source dataset | uspto-grants-2014_01 |
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| ORD ID | ord-04197a26a77e45b48e48162075efe4ed |
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| Source note | uspto-grants-2014_01 |
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