Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Chlorosulfonyl isocyanate | HCID 70918 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 66635412 | HCID 66635412 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 66611538 | HCID 66611538 | — |
Reaction Steps
A solution of 387 mg (1.21 mmol) of the compound of Example 12A in 19.3 ml of acetonitrile was cooled to −15° C., and 148 μl (1.70 mmol) of chlorosulphonyl isocyanate were added. After 5 min, 10 ml of water were added and stirring of the reaction mixture was continued at 60° C. overnight. After cooling to RT, 10 ml of a saturated aqueous sodium bicarbonate solution were added. The mixture was extracted four times with ethyl acetate. The combined organic phases were dried over sodium sulphate and freed from the solvent on a rotary evaporator. 5 ml of a 4 N solution of hydrogen chloride in dioxane were added to the residue and the mixture was stirred for 5 min Once more, the volatile components were then removed on a rotary evaporator. The residue (300 mg, about 90% pure) corresponded to the title compound and was reacted further without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09180120B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-bb786802ff684a09942c9f4c41da85d0 |
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| Source note | uspto-grants-2015_11 |
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