HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1654436Generated: November 1, 2026
Gamma-Aminobutyric Acid → HCID 86748632, compound
https://huagongshe.com/reaction/1654436
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Gamma-Aminobutyric Acid | HCID 119 | — |
| Reactant | Putrescine | HCID 1045 | — |
| Reactant | 3-Aminobenzoic Acid | HCID 7419 | — |
| Reactant | Butylamine | HCID 8007 | — |
| Reactant | Deoxycytidine | HCID 13711 | — |
| Reactant | Deoxyuridine | HCID 13712 | — |
| Reactant | Sodium Bisulfite | HCID 23665763 | — |
| Reactant | HCID 53968575 | HCID 53968575 | — |
| Product | HCID 86748632 | HCID 86748632 | — |
Reaction Steps
Efficient transamination of deoxycytidine is shown to have occurred when the reaction was carried out in the presence of 1M sodium bisulfite and 3M amine at pH 7.2 at a temperature of 48° C. While these conditions can be varied, it is noted that under the conditions used, the nucleoside was converted to 90% or greater of the transaminated product as determined by HPLC analysis. For example, transamination by 4-aminobutyric acid gave 93% of N4 -(3-carboxypropyl)deoxycytidine, 6% deoxyuridine and 1% deoxycytidine. Similar results were obtained when transamination was carried out with 1,4-diaminobutane or 1-aminobutane. Less efficient transamination was observed with 3-aminobenzoic acid, which gave N4 -(3-carboxyphenyl)deoxycytidine in approximately 30%. In this case, the lower extent of reaction appears to be due to the bulky nature of the amine and the lower solubility of the amine which only allowed a 1M solution to be prepared.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05407801 |
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| Source dataset | uspto-grants-1995_04 |
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| ORD ID | ord-2864141cf2394b6db70c22e1b969c7c3 |
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| Source note | uspto-grants-1995_04 |
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