HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1642479Generated: November 1, 2026
Isopropyl chloroformate → HCID 25221223, compound
https://huagongshe.com/reaction/1642479
Participants
| Role | Name | HCID | Charge |
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| Reactant | Isopropyl chloroformate | HCID 7917 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 57619799 | HCID 57619799 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 25221223 | HCID 25221223 | 51% |
Reaction Steps
A solution of (3aR,7aR)-1-[1-(4-methyl-4-piperidyl)-4-piperidyl]-3a,4,5,6,7,7a-hexahydro-3H-benzoimidazol-2-one (HCl salt, 99 mg, 0.25 mmol) and diisopropylethylamine (129.3 mg, 1.0 mmol) in dry dichloromethane (5 mL) at 0° C. was added dropwise with a solution of 1.0 N isopropyl chloroformate in dichloromethane (0.3 mL, 0.3 mmol) and was stirred at room temperature for 3 h. Saturated NaHCO3 (5 mL) was added followed by dichloromethane (20 mL). The phases were separated and the aqueous phase was extracted with dichloromethane (2×10 mL). The combined organic phases were washed with brine, dried over Na2SO4 and concentrated in vacuo. The residue was purified with preparative LC/MS (high pH) to give the title compound (52 mg, 51%). 1H NMR (400 MHz, METHANOL-D4) δ ppm 0.98 (s, 3H), 1.21 (d, J=6.25 Hz, 6H), 1.30-1.51 (m, 6H), 1.61 (d, J=11.33 Hz, 1H), 1.67-1.89 (m, 7H), 1.95 (d, J=7.42 Hz, 1H), 2.13-2.34 (m, 3H), 2.85-3.16 (m, 4H), 3.28-3.41 (m, 2H), 3.47-3.68 (m, 3H), 4.77-4.85 (m, 1H). MS (M+1): 407.3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08119661B2 |
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| Source dataset | uspto-grants-2012_02 |
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| ORD ID | ord-4f4fc179d1af42dc874fc92a80f8c451 |
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| Source note | uspto-grants-2012_02 |
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