HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 881818Generated: November 1, 2026
Trifluoroacetic acid → HCID 68422702, compound
https://huagongshe.com/reaction/881818
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | 2-(4-Methoxy-benzyl)-2H-tetrazole-5-carbonyl chloride | HCID 59607732 | — |
| Reactant | (R)-ethyl 3-amino-4-(3'-chlorobiphenyl-4-yl)butanoate hydrochloride | HCID 86648190 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 68422702 | HCID 68422702 | — |
Reaction Steps
To a solution of intermediate 8-1 in DCM (8 ml) at room temperature is added 2-(4-methoxy-benzyl)-2H-tetrazole-5-carbonyl chloride and followed by TEA (Intermediate 22: 0.293 ml, 2.100 mmol). The reaction is stirred at room temperature for 5 min. The reaction is quenched by brine and is extracted with DCM. The combined organic layer is washed with brine and dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The residue is purified by column chromatography (15% to 40% EtOAc/Heptane). The obtained residue in TFA (5 ml, 64.9 mmol) is heated at 80° C. for 0.5 hours. The reaction is concentrated under reduced pressure to give (R)-4-(3′-chloro-biphenyl-4-yl)-3-[(2H-tetrazole-5-carbonyl)-amino]-butyric acid ethyl ester.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08993631B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-386bfd0e87bd42fbac3257ace83b0289 |
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| Source note | uspto-grants-2015_03 |
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