HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 384518Generated: October 30, 2026
Dichloromethane → (1S,4S)-2,5-Diazabicyclo[2.2.1]heptane-2-carboxamide hydrochloride
https://huagongshe.com/reaction/384518
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Trimethylsilyl isocyanate | HCID 70696 | — |
| Reactant | (1S,4S)-2-Boc-2,5-diazabicyclo[2.2.1]heptane | HCID 11521263 | — |
| Product | (1S,4S)-2,5-Diazabicyclo[2.2.1]heptane-2-carboxamide hydrochloride | HCID 57464029 | — |
Reaction Steps
To a solution of (S,S)-2,5-diaza-bicyclo[2.2.1]heptane-2-carboxylic acid tert-butyl ester (35.6 g, 179 mmol) in CH2Cl2 (600 mL) was added trimethylsilylisocyanate (82.5 g, 716 mmol). After 2 h at rt, the mixture was concentrated, and the resulting white solid was dissolved in CH2Cl2 (500 mL). The solution was then treated with a solution of HCl (4.0 N in 1,4-dioxane, 135 mL). The resulting heterogeneous suspension was then stirred at rt overnight. Upon evaporation of the solvents, the desired product was isolated as a white solid (33 g), which was used directly in the next step. [Note: the mass balance was found to be 104%, which arose from additional HCl that could not be removed by standard evaporation under vacuum]. 1H NMR (500 MHz, CD3OD): 4.77 (s, 1H), 4.55 (s, 1H), 3.69 (d, J=12.1 Hz, 1H), 3.64 (d, J=12.1 Hz, 1H), 3.47 (d, J=11.3 Hz, 1H), 3.40 (d, J=11.3 Hz, 1H), 2.22 (d, J=11.5 Hz, 1H), 2.15 (d, J=11.5 Hz, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08367719B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-9754595601be46b6a3075911ec590298 |
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| Source note | uspto-grants-2013_02 |
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