HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2082687Generated: October 31, 2026
HCID 86735596, compound → HCID 86735595, compound
https://huagongshe.com/reaction/2082687
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 86735596 | HCID 86735596 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 86735595 | HCID 86735595 | — |
| Product | HCID 86735596 | HCID 86735596 | — |
Reaction Steps
A mixture of 0.94 g of benzyl (benzyl 2-acetamido-4-O-acetyl-6-O-triphenylmethyl-α-D-glucopyranosid-3-O-yl)acetyl-L-alanyl-D-isoglutaminate (12C, n = 2, X1 = L-alanyl, R2 = CH3, R3 = --COCH3) and 10 ml of 70% acetic acid is heated at a 100° C until a clear solution is obtained (about 2 minutes) and heating is contained for a further 2 minutes. The solution is immediately cooled in an ice bath and the precipitate is removed by filtration. The filtrate is evaporated to dryness in vacuo, the residue is triturated with 25 ml ether and the resultant solid is collected by filtration, washed with ether and dried in vacuo giving benzyl (benzyl 2-acetamido-4-O-acetyl-α-D-glucopyranosid-3-O-yl)acetyl-L-alanyl-D-isoglutaminate (12C, n = 2, X1 = L-alanyl, R2 = CH3, R3 = COCH3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04082735 |
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| Source dataset | uspto-grants-1978_04 |
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| ORD ID | ord-a5b1bea9391a4ac0a9a1d777671f76b4 |
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| Source note | uspto-grants-1978_04 |
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