HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2269363Generated: November 1, 2026
Trifluoroacetic acid → HCID 70073493, compound
https://huagongshe.com/reaction/2269363
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 70085747 | HCID 70085747 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 70073493 | HCID 70073493 | 98% |
Reaction Steps
To a solution of (2S)-6-benzyloxycarbonylamino-2-tert-butoxycarbonylaminohexanoic acid 1,3,4-thiadiazol-2-ylamide (0.81 g, 1.75 mmol) in dichloromethane (8 mL) is added trifluoroacetic acid (2 mL). The resulting solution is stirred for 4 h at 25° C., is concentrated, diluted with 50 mL of EtOAc, and washed with 1 N aqueous sodium hydroxide solution. The organic layer is dried over anhydrous sodium sulfate and concentrated under reduced pressure to provide (2S)-6-benzyloxycarbonylamino-2-aminohexanoic acid 1,3,4-thiadiazol-2-ylamide as a solid (0.62 g, 98% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06329400B1 |
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| Source dataset | uspto-grants-2001_12 |
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| ORD ID | ord-e5075a3c8fd3469483865e63ff6306e2 |
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| Source note | uspto-grants-2001_12 |
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