HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2169137Generated: November 1, 2026
Hydrochloric Acid → HCID 178484642, compound
https://huagongshe.com/reaction/2169137
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 178484773 | HCID 178484773 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178484642 | HCID 178484642 | 53.33% |
Reaction Steps
To a stirred solution of 5-benzyloxy-2-biphenyl-2-ylmethyl-6-hydroxypyrimidine-4-carboxylic acid [2-(tert-butyl-dimethylsilanyloxy)-ethyl]-methyl-amide (9-01) (2.1 g, 3.602 mmol) in tetrahydrofuran (30 mL) was added 1N HCl (5.4 ml, 5.4 mmol) at room temperature. The mixture was stirred for 60 min at room temperature. After completion of the reaction, the mixture was neutralized with 1N sodium hydroxide aqueous solution, extracted with ethyl acetate, dried over sodium sulfate and concentrated under reduced pressure to get a crude product which was purified using a normal silica column using 60% ethyl acetate in hexane to get 5-benzyloxy-2-biphenyl-2-ylmethyl-6-hydroxypyrimidine-4-carboxylic acid (2-hydroxyethyl)-methyl-amide (10-01) (900 mg, 53.33%) as a floppy light yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09045486B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-3aba0ff0bdc4440d9f237bfc74b9210c |
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| Source note | uspto-grants-2015_06 |
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