HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 622727Generated: November 1, 2026
Bis(2-chloroethyl)amine → N-[N-(cholest-5-en-3beta-oxycarbonyl)glycyl]bis(2-chloroethyl)amine
https://huagongshe.com/reaction/622727
Participants
| Role | Name | HCID | Charge |
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| Reactant | Bis(2-chloroethyl)amine | HCID 9533 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | N-(cholest-5-en-3beta-oxycarbonyl)glycine | HCID 14168269 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-[N-(cholest-5-en-3beta-oxycarbonyl)glycyl]bis(2-chloroethyl)amine | HCID 86742447 | 54.5% |
Reaction Steps
To a solution of N-(cholest-5-en-3β-oxycarbonyl)glycine (160.8 mg) in dry tetrahydrofuran (50 ml) was added said bis(2-chloroethyl)amine (85.2 mg) and dicyclohexylcarbodiimide (61.9 mg) at 0° C. under blowing nitrogen gas and the mixture was stirred for 6 hours. After standing overnight (17 hours) at refrigerator, the reaction mixture was filtered and the solvent was evaporated under reduced pressure. The residue was solved in a mixture of chloroform and methanol (50:1) and was subjected to preparation column chromatography (PLC) eluting with a mixture of chloroform and methanol (50:1). The desired parts were gathered, extracted with a mixture of chloroform and methanol (4:1), filtered and concentrated under reduced pressure to give N-[N-(cholest-5-en-3β-oxycarbonyl)glycyl]bis(2-chloroethyl)amine (110 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04772594 |
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| Source dataset | uspto-grants-1988_09 |
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| ORD ID | ord-bd559e4e847a4eec90e32acf59b57e58 |
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| Source note | uspto-grants-1988_09 |
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