HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 975947Generated: November 1, 2026
Potassium Bromide → HCID 76497815, compound
https://huagongshe.com/reaction/975947
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Bromide | HCID 253877 | — |
| Reactant | HCID 18928063 | HCID 18928063 | — |
| Reactant | Methyl 3-isocyanatophenylacetate | HCID 19070835 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 76497815 | HCID 76497815 | 59.4% |
Reaction Steps
By proceeding in a fashion similar to that described in Example 2, but starting from 6.2 g of tert-butyl (2RS,5SR)-1-(2-aminoacetyl)-5-phenylprolinate in solution in 150 cm3 of anhydrous tetrahydrofuran and 4.2 g of methyl 3-isocyanatophenylacetate, 6 g of methyl (2RS,5SR)-3-{3-[2-(2-tert-butoxycarbonyl-5-phenyl-1-pyrrolidinyl)-2-oxoethyl]ureido}phenylacetate are obtained [proton NMR (200 MHz, DMSO D6, δ in ppm), 2 rotamers at room temperature, peak coalescence at 120° C.: 1.5 (s, 9H, (CH3)3); 3.6 (s, 2H, CH2CO); 3.65 (s, 3H, OCH3); 6.8 to 7.7 (m, 9H, aromatic). Infrared spectrum (KBr), characteristic bands in cm-1 : 3365, 3155, 3110, 3090, 3060, 3030, 2975, 2950, 2930, 2875, 1738, 1700, 1650, 1610, 1595, 1560, 1495, 1435, 1395, 1365, 1315, 1250, 1220, 1155, 1015, 905, 890, 860, 845, 780, 760, 700].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05610144 |
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| Source dataset | uspto-grants-1997_03 |
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| ORD ID | ord-856d8b6f9d724a709b518ac660e4fa9b |
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| Source note | uspto-grants-1997_03 |
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