HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 565250Generated: October 29, 2026
Trifluoroacetic acid → HCID 61148470, compound
https://huagongshe.com/reaction/565250
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Carbamic acid, [(1S)-2,2-dimethyl-1-[[(2-pyridinylmethyl)amino]carbonyl]propyl]-, 1,1-dimethylethyl ester | HCID 70237877 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 61148470 | HCID 61148470 | 100% |
Reaction Steps
To a solution of (2S)-2-tert-butoxycarbonylamino-3,3-dimethylbutanoic acid 2-pyridylmethylamide (16 g, 50 mmol) in dichloromethane (25 mL) cooled at 0° C. is added trifluoroacetic acid (150 mL). The resulting solution is allowed to warm to 25° C. and is stirred for 18 h. The reaction mixture is diluted with toluene, concentrated, brought to pH=10 with 2 M sodium hydroxide, and extracted with 3:1 dichloromethane/isopropanol (200 mL). The organic layer is washed with saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate and concentrated under reduced pressure to provide (2S)-2-Amino-3,3-dimethylbutanoic acid 2-pyridylmethylamide (11 g, 100% yield) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06172064B2 |
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| Source dataset | uspto-grants-2001_01 |
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| ORD ID | ord-7d0e143eb0c948da92f237e62b8c8100 |
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| Source note | uspto-grants-2001_01 |
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