HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 338054Generated: November 3, 2026
Isobutyric Acid → HCID 11411101, compound
https://huagongshe.com/reaction/338054
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isobutyric Acid | HCID 6590 | — |
| Reactant | Diisopropylcarbodiimide | HCID 12734 | — |
| Reactant | HCID 5358230 | HCID 5358230 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Catalyst | Scandium(III) triflate | HCID 2734571 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 11411101 | HCID 11411101 | — |
Reaction Steps
A mixture of maytansinol (6.00 mg, 0.01062 mmol), isobutyric acid (23.60 mg, 0.2124 mmol), Sc(OTf)3 (3.14 mg, 0.00637 mmol) and DMAP (3.89 mg, 0.03186 mmol) in CH2Cl2 (1 mL) was stirred for 0.5 h at −8° C. DIC (29.49 mg, 0.2337 mmol) was added dropwise. The mixture was stirred till completion, quenched with diluted HCl, and extracted with CH2Cl2. The organic layer was washed with aq. NaHCO3, brine, and dried over anhydrous Na2SO4. The solvent was removed under reduced pressure. Chromatography (silica gel, CH2Cl2/MeOH 30:1) gave the desired product ansamitocin P3. LC-MS (M+Na+) calc.: 657.3. found: 657.4.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08889855B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-e29fdcd3fcb947bb9d23f3a6cd9fdff0 |
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| Source note | uspto-grants-2014_11 |
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