HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 45396Generated: October 28, 2026
Benzylamine → 2-(Tert-butoxycarbonylamino)-4-methylthiazole-5-carboxylic acid benzylamide
https://huagongshe.com/reaction/45396
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzylamine | HCID 7504 | — |
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | N-Boc-amino-4-methylthiazole-5-carboxylic acid | HCID 2756770 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-(Tert-butoxycarbonylamino)-4-methylthiazole-5-carboxylic acid benzylamide | HCID 86642521 | 50.1% |
Reaction Steps
To a stirred solution of 2-(tert-butoxycarbonylamino)-4-methylthiazole-5-carboxylic acid (2.97 g, 11.50 mmol) and diisopropylamine (8.5 mL, 48.70 mmol) in dichloromethane (40 mL) was added N-ethyl-N′-(3-dimethylaminopropyl)carbodiimide hydrochloride (2.25 g, 11.50 mmol) and 1-hydroxybenzotriazole (2.02 g, 14.80 mmol). After 30 min benzylamine (1.7 mL, 15.60 mmol) was added. The resultant mixture was stirred at ambient temperature over 8 h, diluted with ethyl acetate, washed with water and brine, dried over anhydrous sodium sulfate, filtered and concentrated in vacuo. The crude product was purified by flash column chromatography eluting with ethyl acetate/hexanes (5/95 to 100/0) to afford 2-(tert-butoxycarbonylamino)-4-methylthiazole-5-carboxylic acid benzylamide (2.00 g, 50% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08541457B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-a0ca25b0155045efa99fa0e55e339a4f |
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| Source note | uspto-grants-2013_09 |
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