HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1534968Generated: October 27, 2026
(+-)-5-Hydroxytryptophan → HCID 136045351, compound
https://huagongshe.com/reaction/1534968
Participants
| Role | Name | HCID | Charge |
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| Reactant | (+-)-5-Hydroxytryptophan | HCID 144 | — |
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | 3-(1,6-dihydro-6-oxo-9H-purin-9-yl)propanoic acid, 4-nitrophenyl ester | HCID 135973957 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 136045351 | HCID 136045351 | 7.3% |
Reaction Steps
100 mg (0.500 mmol) of DL-5-hydroxytryptophan and 3 ml of dry dimethylsulfoxide were placed in a 25 ml round bottom flask equipped with a magnetic stirring bar and stopper. Then 150 mg (0.456 mmol) of 3-(1,6-dihydro-6-oxo-9H-purin-9-yl)propanoic acid, 4-nitrophenyl ester (AIT-0081) were added and the heterogeneous mixture was stirred for 2.5 hours at room temperature in the closed flask. The mixture became completely homogeneous. The reaction mixture was poured into 20 ml of acetone and a semi-solid precipitate was obtained by filtration. The crude product was washed twice with 2 ml of acetone. The solid was resuspended in 10 ml of acetone and the insoluble material was removed by filtration. The acetone solution was evaporated to dryness. The yield of product 2-[[3-(1,6-dihydro-6-oxo-9H-purin-9-yl)-1-oxopropyl]amino]-3-(5-hydroxyl-1H-indol-3-yl)-propionic acid (AIT-0111) was 15 mg. Yield: 7.3% (Purity 93 %).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05091432 |
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| Source dataset | uspto-grants-1992_02 |
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| ORD ID | ord-b67a98265dd44c46b9b57530daeaf694 |
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| Source note | uspto-grants-1992_02 |
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