HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 881992Generated: October 30, 2026
Dimethylformamide → Buprenorphine component OF alks-5461
https://huagongshe.com/reaction/881992
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Bromomethylcyclopropane | HCID 81503 | — |
| Reactant | Norbuprenorphine | HCID 114976 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | Buprenorphine component OF alks-5461 | HCID 9848990 | 56.1% |
Reaction Steps
A mixture of 11.5 g of norbuprenorphine, 4.6 g of sodium bicarbonate, 4.85 g of cyclopropylmethyl bromide (1% butenyl bromide in it by GC) and 46 ml of dry DMF is heated in an oilbath at 80-100° C. for 4 hours until the reaction is substantially complete. The reaction mixture is transferred to a dropping funnel, with minimal DMF as a wash. The reaction mixture is added over 5 minutes to 160 ml of water, with mechanical stirring. (Adding water to the reaction yields a gum). The mixture is stirred for about 10 minutes and filtered. The filter cake is washed with 20 ml water. The HPLC will show about 90% by area of desired product, and 0.2-0.5% of an N-butenyl substituted impurity. The resulting product is dried, yielding about 12 g. The resulting product is boiled in 30 ml of methanol for about 30 minutes, cooled, and filtered to yield about 7.3 g buprenorphine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08993764B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-665878874a614695aa8a58ab4b5d41f8 |
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| Source note | uspto-grants-2015_03 |
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