HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 257272Generated: October 30, 2026
Ethylmorpholine → (R)-N-[(RS)-1-amidino-3-piperidinylmethyl]-alpha(2-naphthylsulfonamido)indole-3-propionamide bisulfite
https://huagongshe.com/reaction/257272
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethylmorpholine | HCID 7525 | — |
| Reactant | Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphate | HCID 151348 | — |
| Reactant | (R)-3-(1H-Indol-3-yl)-2-(naphthalene-2-sulfonylamino)-propionic acid | HCID 1800786 | — |
| Reactant | Rac-3aminomethyl-1-amidinopiperidine sulphite | HCID 19080933 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (R)-N-[(RS)-1-amidino-3-piperidinylmethyl]-alpha(2-naphthylsulfonamido)indole-3-propionamide bisulfite | HCID 22848479 | 44.3% |
Reaction Steps
A solution of 1.5 g of N-(2-naphthylsulfonyl)-D-tryptophan in 30 ml of DMF is treated with 1.5 ml of ethylmorpholine. After the addition of 0.7 g of rac-3-aminomethyl-1-amidinopiperidine sulphite (Example 1) and 1.7 g of benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphate the reaction mixture is stirred for 15 hours. The solvent is evaporated and the residue is taken up in 50 ml of water and extracted with 100 ml of ethyl acetate. The ethyl acetate phase is washed with water, dried and evaporated. The crude material is purified on a RP-18 column with water/acetonitrile (0-30%). There is obtained 0.8 g of (R)-N-[(RS)-1-amidino-3-piperidinylmethyl]-α(2-naphthylsulfonamido)indole-3-propionamide bisulfite, FAB-MS: 533 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05260307 |
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| Source dataset | uspto-grants-1993_11 |
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| ORD ID | ord-be2b33d8263a45e3b3f0c0cb36226db3 |
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| Source note | uspto-grants-1993_11 |
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