HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2054846Generated: October 30, 2026
Isopropyl isocyanate → HCID 59656504, compound
https://huagongshe.com/reaction/2054846
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isopropyl isocyanate | HCID 61277 | — |
| Reactant | 4-Amino-1-Boc-piperidine | HCID 1268291 | — |
| Reactant | Lithium borohydride | HCID 4148881 | — |
| Reactant | HCID 86594774 | HCID 86594774 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 59656504 | HCID 59656504 | — |
Reaction Steps
(±)-(cis)-4-[4-(2-Methyl-benzoylamino)-naphthalene-1-sulfonylamino]-piperidine-1,3-dicarboxylic acid diethyl ester was made following general procedure in Scheme 5, substituting (±)-4-amino-1-benzyl-piperidine-3-carboxylic acid ethyl ester (5) for 4-amino-piperidine-1-carboxylic acid tert-butyl ester, and substituting ethyl chloroformate for 2-isocyanato-propane. To the solution of (±)-(cis)-4-[4-(2-Methyl-benzoylamino)-naphthalene-1-sulfonylamino]-piperidine-1,3-dicarboxylic acid diethyl ester (57 mg, 0.1 mmol) in THF (5 mL), was added lithium borohydride in THF solution (0.5 mL, 0.25 mmol) and the resultant solution was stired at 0° C. for 2 h. The solvent was removed in vacuo and the crude material was purified by HPLC to give the title compound. 1H NMR (300 MHz, MeOD) δ 8.81 (d, 1H), 8.33 (d, 1H), 8.24 (d, 1H), 7.94 (d, 1H), 7.72 (m, 3H), 7.40 (m, 3H), 4.06 (q, 2H), 3.55 (m, 2H), 3.32 (m, 5H), 2.56 (s, 3H), 1.75 (m, 1H), 1.30 (m, 2H), 1.20 (t, 3H); LC/MS m/z 526 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07329755B2 |
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| Source dataset | uspto-grants-2008_02 |
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| ORD ID | ord-284386c9d9394af79df5f055a63af0ac |
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| Source note | uspto-grants-2008_02 |
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