HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 890930Generated: October 29, 2026
Tetrahydrofuran → HCID 69623716, compound
https://huagongshe.com/reaction/890930
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Potassium cyanate | HCID 11378442 | — |
| Reactant | HCID 69623693 | HCID 69623693 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 69623716 | HCID 69623716 | 87% |
Reaction Steps
To a solution of N-(propylsulfonyl)-D-isoleucyl-3-(methylamino)-N1-(4-cyanobenzyl)-L-alaninamide (500 mg, 1.0 mmol) in water (1.3 ml)/tetrahydrofuran (3 ml), potassium cyanate (243 mg, 3 mmol) was added under stirring at 50° C. and then further stirred under the same conditions. After stirring for 3 hours, water was added to the reaction mixture, which was then extracted with ethyl acetate. The ethyl acetate layer was dried over anhydrous magnesium sulfate. Magnesium sulfate was filtered off and the filtrate was concentrated under reduced pressure to give N-(propylsulfonyl)-D-isoleucyl-3-[(aminocarbonyl)(methyl)amino]-N1-(4-cyanobenzyl)-L-alaninamide (430 mg, 0.87 mmol; yield 87%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07001887B2 |
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| Source dataset | uspto-grants-2006_02 |
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| ORD ID | ord-4ad74b1acf7040bd96cb9f6e56f0d6db |
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| Source note | uspto-grants-2006_02 |
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