HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 656256Generated: October 28, 2026
Dimethylformamide → HCID 86639842, compound
https://huagongshe.com/reaction/656256
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Chlorosulfonyl isocyanate | HCID 70918 | — |
| Reactant | HCID 86639843 | HCID 86639843 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86639842 | HCID 86639842 | — |
Reaction Steps
A solution of 1 mmol of tert-butyl (4-((R)-(6-oxaspiro[2.5]-oct-1-yl)carbamoyl)-2-hydroxy-1-(2-[1-(3-methoxypropyl)-1H-indol-6-ylmethyl]-3-methylbutyl)-5-methylhexyl)carbamate in 15 ml of dichloromethane is mixed with 1.5 mmol of chlorosulphonyl isocyanate and stirred at room temperature for 16 hours. 2 ml of N,N-dimethylformamide are added, and the reaction mixture is again stirred for 2 hours. It is quenched with water, and the suspension is vigorously stirred for 10 minutes. It is poured into 1M sodium bicarbonate solution and extracted with ethyl acetate (3×). The combined organic phases are washed with brine, dried with sodium sulphate and evaporated. The title compound is identified by means of the Rf from the residue by flash chromatography (SiO2 60 F).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08071651B2 |
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| Source dataset | uspto-grants-2011_12 |
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| ORD ID | ord-3b9ce8dfc30543d7ad70589ddf5f118c |
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| Source note | uspto-grants-2011_12 |
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